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チオフェン

Thiophene

HCID 8030
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
110-02-1
標準SMILES
c1ccsc1
InChIKey
YTPLMLYBLZKORZ-UHFFFAOYSA-N
分子式
C4H4S
平均分子量
84.14 g/mol
単同位体質量
84.00337113

概要

Thiophene appears as a colorless liquid with an unpleasant odor. Insoluble in water and slightly denser than water. Flash point 30 °F. Vapors heavier than air. Irritates the skin, eyes, and mucous membranes. Used to make pharmaceuticals and dyes.

名称と識別子

優先名称
Thiophene
IUPAC
thiophene
現地名
チオフェン
英語名
Thiophene
分子式
C4H4S
分子量
84.14

名称と別名

THIOPHENE110-02-1ThiofuranThioleThiophenThiotetroleThiacyclopentadieneThiofurfuranDivinylene sulfideThiapheneThiofuramFuran, thio-
名称をさらに表示
チオフェンチオテトロールチオールチオフルフランチオフラン硫化ジビニレンチオフェン, 2000 µg/mL in Tolueneチオフェン, 99%CYP3AthiophenoneHLPcp34THIOPHENE FOR SYNTHESIS 5 MLThiophene, benzene free, extra pure, 99.5%CP33
Huile HSOThiofenHuile H50CP 34USAF EK-1860CCRIS 2935HSDB 130NSC 405073

データベース識別子

CAS
110-02-1
PubChem CID
8030
DTXSID
DTXSID8026145
ChEMBL
CHEMBL278958
ChEBI
CHEBI:30856
UNII
SMB37IQ40B
EC Number
203-729-4
Nikkaji
J1.162.593B、J2.445G

物性

構造計算による物性補完中

XLogP
1.8
極性表面積
28.2 Ų
水素結合供与体数
0
水素結合受容体数
1
回転可能結合数
0
重原子数
5
形式電荷
0
複雑度
22.8

実験および物理化学的性質

Chemical Classes · 2 件

Other Classes -> Thiophenes

Flammable agents - 3rd degree

SpringerMaterials PropertiesCoriolis coupling
LogP · 4 件

log Kow = 1.81

1.81

1.81

1.89

OdorSLIGHT AROMATIC ODOR RESEMBLING BENZENE
Density · 3 件

1.0649 at 68 °F (NTP, 1992) - Denser than water; will sink

1.06494 @ 20 °C/4 °C

Relative density (water = 1): 1.06

Viscosity0.621 mPa.s
Color/FormCOLORLESS LIQUID
Solubility · 6 件

less than 1 mg/mL at 75 °F (NTP, 1992)

MISCIBLE IN ETHANOL, ETHER, ACETONE, AND BENZENE.

SOL IN ALL PROPORTIONS IN ORDINARY ORG SOLVENTS, CARBON TETRACHLORIDE, DIOXANE, PYRIMIDINE, TOLUENE

water solubility = 3,020 mg/l @ 25 °C

3.01 mg/mL at 25 °C

Solubility in water: none

Flash Point · 3 件

30 °F (NTP, 1992)

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 6 件

This chemical does not meet GHS hazard criteria for 1.5% (6 of 391) of reports.

Danger

H225 (98.5%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P273, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 391 reports by companies from 18 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

H402: Harmful to aquatic life [Hazardous to the aquatic environment, acute hazard]

危険有害性情報

Regulatory Information · 5 件

Chemical: Thiophene

Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)

Status: Active Update: 07-02-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/12099

Thiophene: HSNO Approval: HSR001226 Approved with controls

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelFlammable Liquid
Fire Hazards · 3 件

Excerpt from ERG Guide 130 [Flammable Liquids (Water-Immiscible / Noxious)]:

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Highly flammable. Gives off irritating or toxic fumes (or gases) in a fire. Vapour/air mixtures are explosive.

Fire PotentialA VERY DANGEROUS FIRE HAZARD WHEN EXPOSED TO HEAT OR FLAME.
Health Hazards · 2 件

化学と産業

薬理情報

Metabolism/Metabolites · 3 件

THIOPHEN IS METABOLIZED IN VIVO TO PREMERCAPTURIC ACID AND 2-THIENYL-MERCAPTURIC ACID.

RABBITS FED THIOPHEN 150 MG/KG EXCRETED 40% OF DOSE IN URINE IN FORM OF 2 MERCAPTURIC ACIDS, BELIEVED TO BE THIENYL 3-MERCAPTURIC ACID & THIENYL 2-MERCAPTURIC ACID.

MAJOR METABOLITE OF THIOPHENE (200-300 MG/KG, ORALLY) IN RATS & RABBITS WAS 3-HYDROXY-2,3-DIHYDRO-2-THIENYLMERCAPTURIC ACID & 2-THIENYLMERCAPTURIC ACID WAS MINOR METABOLITE. IN RAT 32% OF THIOPHENE EXCRETED UNCHANGED IN EXPIRED AIR & 40% EXCRETED IN URINE AS MERCAPTURIC ACIDS.

Absorption, Distribution and Excretion · 4 件

RABBITS FED THIOPHEN 150 MG/KG EXCRETED ABOUT 35% OF DOSE UNCHANGED IN EXPIRED AIR & 0.5% IN FECES.

(35)S-LABELED THIOPHENE APPLIED TO RABBIT SKIN OR INJECTED IP INTO RATS WAS IMMEDIATELY INCORPORATED INTO SKIN.

(35)S-LABELED THIOPHENE (250 MUCI) ADMIN ONCE SC TO RATS WAS RAPIDLY ABSORBED INTO BLOOD STREAM, DEPOSITED IN MAJOR ORGANS, & EXCRETED WITH URINE. URINE ANAL SHOWED 61.1% OF ISOTOPE WAS EXCRETED WITHIN 34 HR & 74.4% WITHIN 3 DAYS.

FOLLOWING RECTAL & ORAL ADMIN OF (14)C-LABELED THIOPHENE (33 MG/KG), PULMONARY EXCRETION WAS 40% & 5%, RESPECTIVELY.

Cellular LocationsCytoplasm

用途と製造

Uses · 3 件

Used as a solvent, chemical intermediate, and monomer to make copolymers; [HSDB]

ORGANIC SYNTHESIS; COPOLYMERIZES WITH MALEIC ANHYDRIDE

SOLVENT; INT FOR PHARMACEUTICALS, THIOPHENE-PHENOL/FORMALDEHYDE RESINS, AND NEMATOCIDE TETRACHLOROTHIOPHENE

U.S. Production · 2 件

(1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS

(1975) GREATER THAN 4.54X10+5 GRAMS

Methods of Manufacturing · 2 件

MADE AVAILABLE IN COMMERCIAL QUANTITIES BY PROCESS UTILIZING DEHYDROGENATION OF BUTANE WITH SULFUR AS DEHYDROGENATING AGENT, FOLLOWED BY CYCLIZATION WITH SULFUR TO FORM THIOPHENE RING. LAB PREPN BY HEATING SODIUM SUCCINATE WITH PHOSPHORUS TRISULFIDE. ALSO PREPARED BY PASSING ETHYLENE OR ACETYLENE INTO BOILING SULFUR; OR BY PASSING ACETYLENE AND HYDROGEN SULFIDE OVER HOT BAUXITE OR NICKEL HYDROXIDE.

関連反応

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化合物ノート

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30 °F (-1 °C) (CLOSED CUP)

-1 °C

Boiling Point · 4 件

183.9 °F at 760 mmHg (NTP, 1992)

84.0 °C @ 760 MM HG

84.00 °C. @ 760.00 mm Hg

84 °C

Decomposition · 2 件

WHEN HEATED TO DECOMPOSITION IT EMITS HIGHLY TOXIC FUMES OF SULFUR OXIDES.

May be heated to 850 °C without decomposition.

Melting Point · 4 件

-36.8 °F (NTP, 1992)

-39.4 °C

-38.3 °C

-38 °C

物理化学的性質

融点
-38 °C · -38 °C (lit.)
沸点
84 °C · 84 °C (lit.)
比重(密度)
1.051 g/mL · 1.051 g/mL at 25 °C (lit.)
蒸気密度
2.9 · 2.9 (vs air)
蒸気圧
40 mm · 40 mm Hg ( 12.5 °C)
屈折率
20 · n20/D 1.529(lit.)
闪点
-9 °C · -9 °C
貯蔵温度
30 °C · Store below +30°C.
溶解性
四塩化炭素、ヘプタン、ピリミジン、ジオキサン、トルエン、および多くの有機溶媒と混和性 (Keith and Walters, 1992 で引用)
外見
粉
色
クリア
比重
1.06 · 1.06
臭い (Odor)
0.1 %。ネギ科ニンニク · プロピレングリコール中0.10%。ネギ科ニンニク
においのタイプ
硫黄の
由来生物
mouse
臭気閾値(Odor Threshold)
0.00056 ppm · 0.00056ppm
爆発限界(explosive limit)
1.5 · 1.5-12.5%(V)
水溶解度
不溶性
比熱容量
1.47 J/ · Cp(liquid): 1.47 J/(g·K); Cp(gas): 0.87 J/(g·K), at 25℃
Merck
14 · 14,9353
BRN
103222 · 103222
Henry's Law Constant
2.33 and · 2.33 and 2.70 in distilled water and seawater, respectively (Przyjazny et al., 1983)
Dielectric constant
9.3 · 9.3(20℃)
安定性
安定。とても燃えやすい。強力な酸化剤、硝酸塩とは相容れない。
InChI
1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChIKey
YTPLMLYBLZKORZ-UHFFFAOYSA-N
SMILES
c1ccsc1
LogP
1.81 · 1.81-1.86 at pH10
表面張力
26.13 mN/m · 26.13mN/m at 298.15K
CAS データベース
110 · 110-02-1(CAS DataBase Reference)
NISTの化学物質情報
Thiophene(110-02-1)
EPAの化学物質情報
Thiophene (110-02-1)
化学的性質 · 3 件

化学的特性チオフェンは化学式C4H4Sで表される硫黄を含む芳香族化合物の一種です独特の臭いを持ち無色の液体として存在しますこの物質は石油の精製過程や石炭の加工過程で自然に生じることがあり有機化学の分野では重要な役割を果たします

化学的特性Thiophene is a colourless to pale yellow liquid that has an odor similar to benzene. It is a heterocyclic compound with a five-membered ring containing four carbon atoms and one sulfur atom. The ring system is also known as a thienyl ring. It occurs as an impurity in commercial benzene and is used as a solvent and in organic syntheses.

化学性质独特の臭いを有し,化合物の骨格や置換基によっては色を呈する場合がある

Excerpt from ERG Guide 130 [Flammable Liquids (Water-Immiscible / Noxious)]:

· May cause toxic effects if inhaled or absorbed through skin.

Hazards SummaryContact can cause redness of the eyes and skin; Inhalation can cause sore throat, cough and dizziness; [ICSC] May be toxic to the liver; [NJ-HSFS] A skin and eye irritant; May cause liver injury; [MSDSonline]
DOT ID and Guide2414 130
Reactive GroupHydrocarbons, Aromatic
UN ClassificationUN Hazard Class: 3; UN Pack Group: II
Reactivity AlertsHighly Flammable
Reactivity Profile · 1 件

THIOPHENE reacts violently with strong oxidizing agents and concentrated nitric acid causing fire and explosion hazards [Handling Chemicals Safely 1980. p. 899]. A mixture of thiophene and N-nitrosoacetanilide exploded at 0 °C [Ber., 1887, 30, 367].

Chemical DangersDecomposes on heating and on burning. This produces toxic and irritating fumes (sulfur oxides). Reacts violently with oxidizing materials, including fuming nitric acid.

安全と保護具

Fire Fighting · 2 件

Excerpt from ERG Guide 130 [Flammable Liquids (Water-Immiscible / Noxious)]:

Use foam, powder, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 件

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Rest.

Accidental Release Measures · 2 件

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 2 件

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

General First Aid:

Safe StorageFireproof. Separated from oxidizing materials.
Exposure Control and Personal Protection· Wear positive pressure self-contained breathing apparatus (SCBA).
Fire Fighting ProceduresFOAM, CARBON DIOXIDE, DRY CHEMICAL.
Nonfire Spill ResponseExcerpt from ERG Guide 130 [Flammable Liquids (Water-Immiscible / Noxious)]:
Disposal Methods · 1 件

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Spillage Disposal · 1 件

Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Collect leaking liquid in sealable containers. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations. Do NOT wash away into sewer.

Isolation and Evacuation · 2 件

Excerpt from ERG Guide 130 [Flammable Liquids (Water-Immiscible / Noxious)]:

Immediate precautionary measure

Eye PreventionWear safety goggles or eye protection in combination with breathing protection.

毒性情報

Environmental Fate · 3 件

TERRESTRIAL FATE: Based on a recommended classification scheme(1), an estimated Koc value of 230(SRC), determined from an experimental log Kow of 1.81(2) and a recommended regression-derived equation(3), indicates that thiophene is expected to have moderate mobility in soil(SRC). Volatilization of thiophene is expected from moist soil surfaces(SRC) given an estimated Henry's Law constant of 2.9X10-3 atm-cu m/mole(SRC), determined from an experimental vapor pressure of 79.7 mm Hg at 25 °C(4) and water solubility of 3,020 mg/l at 25 °C(5). Volatilization from dry soil surfaces is expected based upon the vapor pressure of this compound(SRC).

AQUATIC FATE: Based on a recommended classification scheme(1), an estimated Koc value of 230, determined from an experimental log Kow of 1.81(2) and a recommended regression-derived equation(3), indicates that thiophene may adsorb to suspended solids and sediment in water(SRC). Thiophene is expected to volatilize from water surfaces(3,SRC) based on an estimated Henry's Law constant of 2.9X10-3 atm-cu m/mole(SRC),determined from an experimental vapor pressure of 79.7 mm Hg at 25 °C(4) and water solubility of 3,020 mg/l at 25 °C(5). Estimated half-lives for a model river and model lake are 3 and 89, hours respectively(6,SRC). According to a classification scheme(7), experimental BCF values in the range of 2-7 measured for carp(8), suggests that bioconcentration in aquatic organisms is low(SRC). Biodegradation is not expected to be an important fate process for this compound(SRC). Using a standard BOD dilution technique and an activated sludge inoculum, a theoretical BOD of 0% was observed during a 2 week incubation period(8). No biodegradation was observed when thiophene was incubated in an aquifer slurry for a period of 1 year(9).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), thiophene, which has an experimental vapor pressure of 79.7 mm Hg at 25 °C(2), will exist solely as a vapor in the ambient atmosphere. Vapor-phase thiophene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals and nitrate radicals with experimental atmospheric half-life of about 40 hours and 2.5 nighttime hours, respectively(SRC).

Food Survey ValuesThiophene was detected in the volatiles of Idaho Russet baked potatoes(1) and meat volatiles(2).
Adverse EffectsOccupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Exposure RoutesThe substance can be absorbed into the body by inhalation of its vapour.
Signs and Symptoms · 3 件

Cough. Dizziness. Sore throat.

Redness.

Redness. Pain.

Ongoing Test Status · 1 件

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=110-02-1]

Effluent Concentrations · 1 件

Thiophene was detected, not quantified, in the gas emissions of a Norwegian waste incinerator(1). Thiophene was detected at concentrations of 20-620 ppb in the leachate of a shale oil processing facility(2). Thiophene was detected in air samples above wastewater from shale oil processing facilities in Colorado and Utah at concentrations of 1-10 ng/l(3).

Soil Adsorption/Mobility · 1 件

The Koc of thiophene is estimated as approximately 230(SRC), using a measured log Kow of 1.81(1) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that thiophene is expected to have moderate mobility in soil(SRC).

Natural Pollution SourcesNaturally occurring source of thiophene is petroleum(1,2).
Human Toxicity ExcerptsIn man, tiophene has caused skin irritation and may induce sensitization responses. Nausea, itching and jaundice were seen in a woman repeatedly taking thiophene in suppositories.
Artificial Pollution SourcesThiophenes's production and use as an organic synthesis reagent and solvent(1,2) may result in its release to the environment through various waste streams(SRC).
Environmental Biodegradation · 1 件

Biodegradation is not expected to be an important environmental fate process for thiophene(SRC). No biodegradation was observed when thiophene was incubated in an anoxic aquifer slurry for a period of 3 months(1). Using a standard BOD dilution technique and an activated sludge inoculum, a theoretical BOD of 0% was observed during a 2 week incubation period(2). No biodegradation was observed when thiophene was incubated in an aquifer slurry for a period of 1 year(3).

安全データ

wgk
3
tsca
TSCA listed
rtecs
XM7350000
ridadr
UN 2414
毒性
LD50 orally in Rabbit: 1400 mg/kg
hs_code
29349990
risk_code
45-46-11-20/21/22-41-52/53-36-20/22-37/38-22-48/20/21/22
化審法
(9)-810
消防法
危-4-1-II
hazard_code
F,Xn,Xi,T
hazard_note
Irritant/Highly Flammable
safety_code
53-26-39-45-61-36/37/39-16-36
hazard_class
3
packing_group
II
自然発火温度
743 °F
Hazard Classifications
Acute Tox. 4 OralAquatic Chronic 3Eye Irrit. 2Flam. Liq. 2
ストレージクラス
3 - Flammable liquids
有毒物質データの
110-02-1(Hazardous Substances Data)

FROM...PETROLEUM; SYNTHETICALLY FROM HEATING SODIUM SUCCINATE WITH PHOSPHORUS TRISULFIDE.

General Manufacturing Information · 6 件

Thiophene: ACTIVE

THIOPHENE IS A SULFUR-CONTAINING FLAVOR COMPOUND FORMED BY MAILLARD REACTIONS IN HEAT-PROCESSED COFFEE AND BEEF. /FROM TABLE/

/THIOPHENE IS A/ SOLVENT SIMILAR TO BENZENE, BUT SUITABLE FOR LOWER & HIGHER TEMPERATURES...

STUDIES WERE CONDUCTED ON DEODORIZATION CATALYSTS. THIOPHENE WAS USED AS MODEL IN LOW CONCN RANGE.

MILK XANTHINE OXIDASE CATALYZED THE OXIDATION OF CROTONALDEHYDE WHEN PRESENT AS A SUSPENSION IN THIOPHENE OR IN OTHER NONPOLAR SOLVENTS.

FOUND IN COAL TAR, IN COAL GAS & TECHNICAL BENZENE.

応用分野 · 5 件

解説チオフェンとは、硫黄を環内に持つ五員環複素環式化合物の1つです。 チオフェンという名前は、硫黄を示す接頭語のチオ (英: thio) とを示すフェン (英: phene) を合わせて命名されています。チオール (英: thiole) と呼ばれることもありますが、チオール (英: thiol) と紛らわしいため推奨されていません。 チオフェンは、タールや石炭ガス中に少量含まれています。また、工業的には、高温環境下でブタンと硫黄を脱水素閉環反応により合成されます。

用途ベンゼンと同様の溶剤(高温及び低温に適する)、樹脂、染料、医薬品。

使用Thiophene is used as a building block of various organic molecules and pharmaceuticals providing functional properties.

一般的な説明Thiophene appears as a colorless liquid with an unpleasant odor. Insoluble in water and slightly denser than water. Flash point 30 °F. Vapors heavier than air. Irritates the skin, eyes, and mucous membranes. Used to make pharmaceuticals and dyes.

使用用途チオフェンは溶媒として用いられる他、染料・プラスチック・医農薬の原料としても利用されています。少数のチオフェンが重合したオリゴチオフェンとその機能性誘導体は、有機ELや有機電界効果トランジスタ、有機太陽電池などのハイテク用途として、幅広く使用可能です。 また、多数のチオフェンが連なった構造のポリチオフェンは、導電性高分子として使用されています。チオフェンを原料として合成される縮環チオフェンは、高性能なとして、高移動度トランジスタや有機薄膜太陽電池、有機ELなどの電子デバイスに欠かせない物資です。

調製方法 · 2 件

Thiophene is present in coal tar and is recovered in the benzene distillation fraction (up to about 0.5% of the benzene present). Its removal from benzene is accomplished by mixing with concentrated sulfuric acid, soluble thiophene sulfonic acid being formed. Thiophene gives a characteristic blue coloration with isatin in concentrated sulfuric acid. The basic nomenclature of the thiophene ring system and its derivatives is indicated by the following: the sulfur atom is number 1, positions 2 and 5 are equivalent in the parent ring, as are the 3 and 4 positions.

純化方法The simplest purification procedure is to dry thiophen with solid KOH, or reflux it with sodium, and fractionally distil it through a glass-helices-packed column. More extensive treatments include an initial wash with aqueous HCl, then water, drying with CaSO4 or KOH, and passage through columns of activated silica gel or alumina. Fawcett and Rasmussen [J Am Chem Soc 67 1705 1945] washed thiophene successively with 7M HCl, 4M NaOH, and distilled water, dried with CaCl2 and fractionally distilled it. *Benzene was removed by fractional crystallisation by partial freezing, and the thiophene was degassed and sealed in Pyrex flasks. [Also a method is described for recovering the thiophene from the *benzene-enriched portion.] [Beilstein 17 H 29, 17 I 17, 17 II 35, 17 III/IV 234, 17/1 V 297.]

上流・下流製品情報

上流原料

Motor benzolSolid sodium hydroxideMethylthiopheneコールタールナフサブタン三硫化二リン

下流製品

5-Oxo-5-(2-thienyl)valeric acidジ(2-チエニル)ケトン4-(2-チエニル)ブタン酸2-(トリメチルアセチル)チオフェンピランテル2-ヨードチオフェンノコダゾール4-(2-チエニル)ベンズアルデヒドヘキシル2-チエニルケトンチオフェン-2-スルホニルクロリドγ-オキソ-2-チオフェン酪酸2-チエニルメチルアミン(4-Amino-3-nitrophenyl)-(2-thienyl)methanone2-ベンゾイルチオフェン2,2,2-トリフルオロ-1-(チオフェン-2-イル)エタノンチオフェン-2-酢酸2-(4-ブロモフェニル)チオフェン5-(2-チエニル)ペンタン酸2-(5-ブロモチエン-2-イル)ピリジン(4-Methoxy-3-nitrophenyl)-(thiophen-2-yl)methanone ,98%2-チエニル(4-メトキシフェニル)ケトン
補足説明 · 1 件

定義ChEBI: Thiophene is a monocyclic heteroarene that is furan in which the oxygen atom is replaced by a sulfur. It has a role as a non-polar solvent. It is a mancude organic heteromonocyclic parent, a member of thiophenes, a monocyclic heteroarene and a volatile organic compound.