기본 정보
- 표준 SMILES
Cc1ccsc1Br- InChIKey
YYJBWYBULYUKMR-UHFFFAOYSA-N- 분자식
- C5H5BrS
- 평균 분자량
- 177.06 g/mol
- 단동위원소 질량
- 175.92953326
이름 및 식별자
- 우선 이름
- 2-Bromo-3-methylthiophene
- IUPAC
- 2-bromo-3-methylthiophene
- 영어명
- 2-Bromo-3-methylthiophene
- 분자식
- C5H5BrS
- 분자량
- 177.06
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
14282-76-9- PubChem CID
- 84314
- DTXSID
DTXSID20162194- EC Number
- 238-175-2
- Nikkaji
- J149.674C
물성
구조 계산 물성
- XLogP
- 3
- 극성 표면적
- 28.2 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 1
- 회전 가능 결합 수
- 0
- 무거운 원자 수
- 7
- 형식 전하
- 0
- 복잡도
- 65.1
실험 및 물리화학적 성질
물리화학적 성질
- 녹는점
- 25 °C · <25 °C
- 끓는 점
- 173 · 173-176 °C (lit.)
- 밀도
- 1.572 g/mL · 1.572 g/mL at 25 °C (lit.)
- 굴절률
- 20 · n20/D 1.572(lit.)
- 인화점
- 155 °F · 155 °F
- 저장 조건
- 2 · 2-8°C
- 수용성
- 물에 불용성
- 용해도
- soluble in Chloroform, Ethyl Acetate
- 물리적 상태
- 액체
- 색상
- 옅은 노랑
- Specific Gravity
- 1.58 · 1.580
- BRN
- 105719 · 105719
- InChI
- InChI=1S/C5H5BrS/c1-4-2-3-7-5(4)6/h2-3H,1H3
- InChIKey
- YYJBWYBULYUKMR-UHFFFAOYSA-N
- SMILES
- C1(Br)SC=CC=1C
- NIST
- 2 · Thiophene, 2-bromo-3-methyl-(14282-76-9)
화학적 성질
clear colorless to light yellow liquid
안전 및 규제
GHS 분류
GHS Classification
Danger
H302 (97.8%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P330, P332+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 46 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
안전 데이터
- wgk
- 3
- ridadr
- UN 2810
- HS 번호
- 29349990
- risk_code
- 25-41-43-36/37/38-20/21/22
- hazard_code
- T,Xi,Xn
- safety_code
- 26-36/37/39-45
- 포장분류
- III
- 위험 등급
- 6.1
- 위험 참고 사항
- Harmful
화학 및 산업
응용 분야
용도2-Bromo-3-methylthiophene was used in the preparation of poly(3,3′′′-dimethyl-(2,2′:5′,2′:5′,2′′′)tetrathiophene)). It was also used in the preparation of 2-bromo-3-(bromomethyl)thiophene, lachrymatory compound.
일반 설명2-Bromo-3-methylthiophene is formed (approx. 90%) by bromination of 3-methyl thiophene with N-bromosuccinimide in the absence of benzoyl peroxide.
제조 방법
2-Bromo-3-methylthiophene synthesis: To a solution of glacial AcOH (100 mL), acetic anhydride (4.0 g, 0.039 mol), and 3-methylthiophene (9.82 g, 0.100 mol) as a stirred mixture was added NBS (19.6 g, 0.11 mol) in one portion with a slight exotherm to 44 oC. After 20 min the reaction mixture was poured onto ice, neutralized with sodium bisulfite and extracted with ether. The ether layer was washed with water and concentrated to give 11.3 g (64%) of 2-bromo-3-methylthiophene as a tan colored liquid in 88% purity by GC area % analysis: 1H NMR (CDCl3) d 7.1 (d, 1H, J=5.7 Hz), 6.7 (d, 1H, J=5.9 Hz), 2.2 (s, 3H).
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