1,1'-チオカルボニルジイミダゾール

1,1'-Thiocarbonyldiimidazole

HCID 80264CAS 6160-65-2

基本情報

標準SMILES
S=C(n1ccnc1)n1ccnc1
InChIKey
RAFNCPHFRHZCPS-UHFFFAOYSA-N
分子式
C7H6N4S
平均分子量
178.22 g/mol
単同位体質量
178.03131719

名称と識別子

優先名称
1,1'-Thiocarbonyldiimidazole
IUPAC
di(imidazol-1-yl)methanethione
現地名
1,1'-チオカルボニルジイミダゾール
英語名
1,1'-Thiocarbonyldiimidazole
分子式
C7H6N4S
分子量
178.21

名称と別名

1,1'-ThiocarbonyldiimidazoleRefChem:8977676160-65-2ThiocarbonyldiimidazoleN,N'-Thiocarbonyldiimidazoledi(imidazol-1-yl)methanethionedi(1H-imidazol-1-yl)methanethione1,1-ThiocarbonyldiimidazoleMFCD000052891H-Imidazole, 1,1'-carbonothioylbis-N,N-ThiocarbonyldiimidazoleTCDI
名称をさらに表示
1,1'-チオカルボニルジイミダゾール1,1'-(チオキソメチレン)ビス(1H-イミダゾール)ジ(1H-イミダゾール-1-イル)チオケトンビス(1H-イミダゾール-1-イル)チオケトンビス(1-イミダゾリル)チオケトン1,1'-(チオカルボニル)ビス(1H-イミダゾール)1,1'-カルボノチオイルビス(1H-イミダゾール)1,1’-(チオカルボニル)ビス(1Hイミダゾル)1,1′‐(チオカルボニル)ビス(1H‐イミダゾ-ル)1,1′-チオカルボニルジイミダゾール1,1'-カルボノチオイルビス-1H-イミダゾールチオカルボニルジイミダゾール1,1-チオカルボニルジイミダゾール1,1'-チオカルボニルジイミダゾール, TEC1,1'-チオカルボニルジイミダゾール, tech 90%1,1′-カルボノチオイルジ(1H-イミダゾール)1,1′-(チオカルボニル)ビス(1H-イミダゾール)1,1′-カルボノチオイルビス(1H-イミダゾール)ビス(1H-イミダゾール-1-イル)メタンチオン1-(1H-イミダゾール-1-カルボチオイル)-1H-イミダゾールThiocarbonyl diimidazolebis(1H-imidazol-2-yl)methanethioneDiiMidazdiimidazoL1,1'-THIOCARBONYL1,1'-Thiocarbonyldii
Thiocarbonylbisimidazole1,1'-Thiocarbonylbis(imidazole)Di-1H-imidazol-1-ylmethanethione1,1'-Carbonothioylbis-1H-imidazoleH8A75XB5AY1,1'-(Thiocarbonyl)diimidazole1-(1H-imidazole-1-carbothioyl)-1H-imidazoledi-1H-imidazol-1-ylmethanethion

データベース識別子

CAS
6160-65-2
PubChem CID
80264
DTXSID
DTXSID70210614
UNII
H8A75XB5AY
EC Number
228-183-4
Nikkaji
J5.204C

物性

構造計算による物性

XLogP
0.7
極性表面積
67.7 Ų
水素結合供与体数
0
水素結合受容体数
3
回転可能結合数
0
重原子数
12

実験および物理化学的性質

Chemical ClassesNitrogen Compounds -> Imidazoles
Physical DescriptionYellow powder; [Alfa Aesar MSDS]

物理化学的性質

融点
98 · 98-102 °C(lit.)
沸点
342 °C · 342°C (rough estimate)
比重(密度)
1.3046 · 1.3046 (rough estimate)
屈折率
1.55 · 1.5500 (estimate)
貯蔵温度
2 · 2-8°C
溶解性
テラヒドロフラン、トルエン、ジクロロメタンに可溶。

化学的性質

化学的特性yellow powder

安全と法規制

GHS分類

GHS Classification · 5 件

This chemical does not meet GHS hazard criteria for 6.7% (1 of 15) of reports.

Warning

H302 (53.3%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 15 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory Information · 3 件

Chemical: 1H-Imidazole, 1,1'-carbonothioylbis-

Status: No longer Valid Update: 03-12-2020 https://echa.europa.eu/registration-dossier/-/registered-dossier/32005

1H-Imidazole, 1,1'-carbonothioylbis-: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationEvaluation - Chemicals not considered for in depth evaluation - Not commercially active in Australia
Hazards SummaryAn irritant; Harmful by ingestion; [Alfa Aesar MSDS]
Hazard Classes and CategoriesAcute Tox. 4 (53.3%)

安全データ

F
9-21
wgk
3
hs_code
29332900
risk_code
22-34
hazard_code
Xi
hazard_note
Irritant/Keep Cold/Moisture Sensitive

化学と産業

応用分野 · 2 件

説明1,1'-Thiocarbonyldiimidazole (TCDI) is an imidazole compound that can be prepared by reacting thiophosphoryl chloride with two corresponding imidazoles. Its structure has two imidazole rings, and the imidazole groups can be rapidly displaced, making it a safer alternative to thiophosphoryl chloride. TCDI is used as an organic synthesis or chemical reaction reagent for the synthesis of thiosemicarbazones and thioamides. It is also used in the Corey-Winter olefin synthesis and in the Barton-McCombie deoxygenation reaction. In addition, it is the sulfur analogue of the peptide addition reagent carbodiimidazole (CDI), which is used to couple peptides.

使用1,1'-Thiocarbonyldiimidazole is used as a reagent for the deoxygenation of alcohols with tributyltin hydride and diols with lithium aluminum hydride. It is also used to deoxygenate carboxylic monosaccharide analogues. Further, it is a useful reagent involved in biochemical synthesis. In addition to this, it is used to prepare 1-[bis-(4-methoxy-phenyl)-methyl]-1H-imidazole by reacting with 4,4'-dimethoxy-benzhydrol.

調製方法 · 1 件

純化方法It forms yellow crystals on recrystallisation from tetrahydrofuran or by sublimation at 10-3torr (bath temperature 70-80o). It is hydrolysed by H2O and should be stored dry. [Staab & Walther Justus Liebigs Ann Chem 657 98 1962; Pullukat et al. Tetrahedron Lett 1953 1967, Hanessian et al. Can J Chem 65 1859 1987, Rajanbabu et al. J Am Chem Soc 111 1759 1989.] Thiochrome {2,7-dimethyl-5H -thiachromine-8-ethanol; 3,8-dimethyl-2-hydroxyethyl-5H -

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