기본 정보
- 표준 SMILES
Brc1ccc(-c2cccs2)s1- InChIKey
OMOAIGVIYUXYAU-UHFFFAOYSA-N- 분자식
- C8H5BrS2
- 평균 분자량
- 245.2 g/mol
- 단동위원소 질량
- 243.90161
이름 및 식별자
- 우선 이름
- 5-Bromo-[2,2']bithiophenyl
- IUPAC
- 2-bromo-5-thiophen-2-ylthiophene
- 현지명
- 5-브로모-22'-비티오펜96
- 영어명
- 5-BROMO-2 2'-BITHIOPHENE 96
- 분자식
- C8H5BrS2
- 분자량
- 245.16
이름 및 동의어
5-Bromo-[2,2']bithiophenyl5-Bromo-(2,2')bithiophenylRefChem:532639871-109-65-bromo-2,2'-bithiophene3480-11-32-bromo-5-thiophen-2-ylthiophene2-BromodithiopheneMFCD01461947C8H5BrS25-Bromo-2,2 inverted exclamation marka-bithiophene2,2'-bithiophene, 5-bromo-
이름 더 보기
5-브로모-22'-비티오펜962T-Br5-Bromo-alpha-dithienyl5-BroMo-2,2'-bithiophene 96%5-BROMO-2 2'-BITHIOPHENE 965-Bromo-2,2'-bithiophene USP/EP/BP5-Bromo-2,2′-bithiophene, CAS 3480-11-3
5-bromo-2,2'-bithienylSCHEMBL196515SCHEMBL55415062-bromo-5-(2-thienyl)thiophene5-bromo-2-(2-thienyl)thiopheneDTXSID00348691OMOAIGVIYUXYAU-UHFFFAOYSA-N5-Bromo-2,2'-bithiophene, 96%
데이터베이스 식별자
- CAS
3480-11-3- PubChem CID
- 640065
- DTXSID
DTXSID00348691- EC Number
- 871-109-6
- Nikkaji
- J1.013.246K
물성
구조 계산 물성
- XLogP
- 4
- 극성 표면적
- 56.5 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 1
- 무거운 원자 수
- 11
- 형식 전하
- 0
- 복잡도
- 140
물리화학적 성질
- 녹는점
- 29 · 29-32 °C(lit.)
- 끓는 점
- 50 °C · 50 °C(Press: 0.006 Torr)
- 밀도
- 1.635 · 1.635±0.06 g/cm3(Predicted)
- 인화점
- 230 °F · >230 °F
- 저장 조건
- Keep in dark place,Sealed in dry,Room Temperature
- 물리적 상태
- solid
- InChI
- 1S/C8H5BrS2/c9-8-4-3-7(11-8)6-2-1-5-10-6/h1-5H
- InChIKey
- OMOAIGVIYUXYAU-UHFFFAOYSA-N
- SMILES
- Brc1ccc(s1)-c2cccs2
안전 및 규제
GHS 분류
GHS ClassificationNot Classified;Reported as not meeting GHS hazard criteria by 1 of 1 companies. For more detailed information, please visit ECHA C&L website.
유해성 정보
Hazard Classes and CategoriesNot Classified
안전 데이터
- wgk
- 3
- 스토리지 클래스
- 11 - Combustible Solids
화학 및 산업
응용 분야
용도5-Bromo-2,2′-bithiophene may be used in the synthesis of trimethyl-[2,2′;5′,2″;5″,2″]quaterthiophen-5-yl-silane (4TTMS) and 5-hexylsulfanyl-2,2′:5′,2′′-terthiophene.
일반 설명5-Bromo-2,2′-bithiophene is a bromothiophene derivative. Its reaction with various aryl iodides bearing an electron-donating or electron-withdrawing substituent has been described. It can be synthesized from 2,2′-bithiophene.
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