기본 정보
- 표준 SMILES
Fc1cccc2ccccc12- InChIKey
CWLKTJOTWITYSI-UHFFFAOYSA-N- 분자식
- C10H7F
- 평균 분자량
- 146.16 g/mol
- 단동위원소 질량
- 146.05317844
개요
1-fluoronaphthalene appears as needles. (NTP, 1992)
이름 및 식별자
- 우선 이름
- 1-Fluoronaphthalene
- IUPAC
- 1-fluoronaphthalene
- 영어명
- 1-Fluoronaphthalene
- 분자식
- C10H7F
- 분자량
- 146.16
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
321-38-0- PubChem CID
- 9450
- DTXSID
DTXSID7059808- UNII
- 0920702UT7
- EC Number
- 206-287-0
- Nikkaji
- J9.228B
물성
구조 계산 물성
- XLogP
- 3.7
- 극성 표면적
- 0 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 1
- 회전 가능 결합 수
- 0
- 무거운 원자 수
- 11
- 형식 전하
- 0
- 복잡도
- 133
실험 및 물리화학적 성질
Physical Description
1-fluoronaphthalene appears as needles. (NTP, 1992)
CBI
Solid; [CAMEO] Colorless liquid; [Alfa Aesar MSDS]
물리화학적 성질
- 녹는점
- -13 °C · -13 °C (lit.)
- 끓는 점
- 215 °C · 215 °C (lit.)
- 밀도
- 1.1322 g/mL · 1.1322 g/mL at 20 °C (lit.)
- 굴절률
- 20 · n20/D 1.593(lit.)
- 인화점
- 150 °F · 150 °F
- 저장 조건
- Sealed in dry,Room Temperature
- 용해도
- 물에 약간 용해되고 클로로포름, 에틸 아세테이트 및 메탄올에 잘 용해됩니다.
- 물리적 상태
- 기름
- 색상
- 무색~황색
- Specific Gravity
- 1.332 · 1.332
- 수용성
- 물에 섞이거나 혼합하기 어렵지 않습니다.
- BRN
- 1906413 · 1906413
- 안정성
- 안정적인. 강한 산화제와 호환되지 않습니다.
- InChI
- 1S/C10H7F/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H
- InChIKey
- CWLKTJOTWITYSI-UHFFFAOYSA-N
- SMILES
- Fc1cccc2ccccc12
- NIST
- 1 · Naphthalene, 1-fluoro-(321-38-0)
- EPA
- 1 · 1-Fluoronaphthalene (321-38-0)
화학적 성질
clear slightly yellow to yellow-brown liquid
안전 및 규제
GHS 분류
GHS Classification
This chemical does not meet GHS hazard criteria for 5.5% (3 of 55) of reports.
Warning
H315 (94.5%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 55 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
Regulatory Information
Naphthalene, 1-fluoro- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Naphthalene, 1-fluoro- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 05-12-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/18128
Reactivity Profile
Simple aromatic halogenated organic compounds, such as 1-FLUORONAPHTHALENE, are very unreactive. Halogenated organics generally become less reactive as more of their hydrogen atoms are replaced with halogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
안전 및 보호
First Aid
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.
Nonfire Spill Response
SMALL SPILLS AND LEAKAGE: If you spill this chemical, use absorbent paper to pick up all liquid spill material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
Personal Protective Equipment (PPE)
RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter.
안전 데이터
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- QJ7100000
- ridadr
- UN2810
- HS 번호
- 29039990
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26-36
- 위험 등급
- IRRITANT
- 위험 참고 사항
- Flammable
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
- 스토리지 클래스
- 10 - Combustible liquids
화학 및 산업
용도 및 제조
General Manufacturing Information
All Other Basic Organic Chemical Manufacturing
Naphthalene, 1-fluoro-: ACTIVE
응용 분야
용도1-Fluoronaphthalene is a fluorinated naphthalene derivative that is metabolized by fungal monooxygenase-epoxide hydrolase. It is also used as a pharmaceutical intermediate. It is Duloxetine impurity.
제조 방법
The preparation of 1-Fluoronaphthalene is as follows:1) Diazotization reaction: 1500 g of hydrochloric acid (mass concentration: 25%) and 300 g of naphthylamine were added to a 3000 mL three-necked flask, stirred and heated to 75 ° C to dissolve, and the temperature was lowered to below 5 ° C, and 148 g was slowly added at this temperature. Sodium nitrite, stirred at low temperature for 0.3 hours after the addition, to obtain a diazonium salt solution;2) Substitution reaction: 360 g of fluoroboric acid solution (concentration: 45%) was added to the resulting solution obtained in the step 1), stirred for 0.25 h, filtered, and the filter cake was dried at a temperature of 50 ° C for 0.2 h to obtain Dry naphthylamine diazonium salt fluoroborate double salt;3) Hot air decomposition: the dried diazonium salt fluoroborate double salt is slowly added to the reactor through which hot air (hot air temperature is 85-90 ° C), and the dried powdered naphthylamine diazonium salt fluoroborate double salt is The hot air blows up the dispersion and absorbs the heat for thermal decomposition to obtain a 1-fluoronaphthalene solution containing a small amount of solid impurities;4) Purification treatment: the 1-fluoronaphthalene solution obtained in the step 3) is first washed with pure water for 3 to 6 times, then neutralized with a soda ash to a pH of 6.8 to 7.2, and finally the oil layer is separated by filtration, and the filtrate is taken. The distillation treatment gave 210 g of a naphthalene-based fluorine-containing intermediate 1-fluoronaphthalene in an amount of 99.8%.
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