기본 정보
- 표준 SMILES
C[Si](C)(C)C(Cl)[Si](C)(C)C- InChIKey
XNJGZHVYPBNLEB-UHFFFAOYSA-N- 분자식
- C7H19ClSi2
- 평균 분자량
- 194.85 g/mol
- 단동위원소 질량
- 194.07138135
이름 및 식별자
- 우선 이름
- Bis(trimethylsilyl)chloromethane
- IUPAC
- [chloro(trimethylsilyl)methyl]-trimethylsilane
- 영어명
- Bis(trimethylsilyl)chloromethane
- 분자식
- C7H19ClSi2
- 분자량
- 194.85
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
5926-35-2- PubChem CID
- 552583
- DTXSID
DTXSID80339002- EC Number
- 628-127-2
- Nikkaji
- J46.932G
물성
구조 계산 물성
- 극성 표면적
- 0 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 0
- 회전 가능 결합 수
- 2
- 무거운 원자 수
- 10
- 형식 전하
- 0
- 복잡도
- 95.8
실험 및 물리화학적 성질
물리화학적 성질
- 끓는 점
- 57 · 57-60 °C/15 mmHg (lit.)
- 밀도
- 0.892 g/mL · 0.892 g/mL at 25 °C (lit.)
- 굴절률
- 20 · n20/D 1.449(lit.)
- 인화점
- 120 °F · 120 °F
- 용해도
- soluble in common organic solvents (DMF, THF, Et2O, CH2Cl2).
- 물리적 상태
- liquid
- Specific Gravity
- 0.892 · 0.892
- BRN
- 1736681 · 1736681
- InChI
- 1S/C7H19ClSi2/c1-9(2,3)7(8)10(4,5)6/h7H,1-6H3
- InChIKey
- XNJGZHVYPBNLEB-UHFFFAOYSA-N
- SMILES
- C[Si](C)(C)C(Cl)[Si](C)(C)C
안전 및 규제
GHS 분류
GHS Classification
Warning
H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, 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 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
안전 데이터
- wgk
- 3
- tsca
- No
- ridadr
- UN 1993 3/PG 3
- risk_code
- 10-36/37/38
- hazard_code
- Xi
- safety_code
- 26-36/37/39
- 포장분류
- III
- 위험 등급
- 3.2
- F 고인화성물질
- 21
- Hazard Classifications
- Eye Irrit. 2Flam. Liq. 3Skin Irrit. 2STOT SE 3
- 스토리지 클래스
- 3 - Flammable liquids
화학 및 산업
응용 분야
용도Silane, 1,1-(Chloromethylene)bis[1,1,1]- trimethyl- can be used as versatile C1 building block; broad application in Peterson olefination reactions; Grignard reagent participates readily in Kumada cross-coupling reactions with aryl and vinyl halides; useful in synthesis of methylenephosphine analogs and as sterically demanding ligand for a number of main group and transition metal complexes.
제조 방법
a convenient one-pot procedure has been developed by Kemp and Cowley in which trimethylsilylchloride reacts with dichloromethane in the presence of nBuLi at 110°Cto give bis(trimethylsilyl)dichloromethane.1 This intermediate is sequentially treated with nBuLi and ethanol to yield chlorobis(trimethylsilyl)methane. A number of other syntheses have been described
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