기본 정보
- 표준 SMILES
C[Si](C)(C)I- InChIKey
CSRZQMIRAZTJOY-UHFFFAOYSA-N- 분자식
- C3H9ISi
- 평균 분자량
- 200.09 g/mol
- 단동위원소 질량
- 199.95182482
개요
structure in first source
이름 및 식별자
- 우선 이름
- Trimethylsilyl iodide
- IUPAC
- iodo(trimethyl)silane
- 현지명
- 요오드트리메틸실란
- 영어명
- Iodotrimethylsilane
- 분자식
- C3H9ISi
- 분자량
- 200.09
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
16029-98-4- PubChem CID
- 85247
- DTXSID
DTXSID4065997- UNII
- 7A65KRZ6NV
- EC Number
- 240-171-0
- Nikkaji
- J150.775C
물성
구조 계산 물성
- 극성 표면적
- 0 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 0
- 회전 가능 결합 수
- 0
- 무거운 원자 수
- 5
- 형식 전하
- 0
- 복잡도
- 28.4
실험 및 물리화학적 성질
물리화학적 성질
- 녹는점
- 0 °C · <0°C
- 끓는 점
- 106 °C · 106 °C(lit.)
- 밀도
- 1.406 g/mL · 1.406 g/mL at 25 °C(lit.)
- 굴절률
- 20 · n20/D 1.471(lit.)
- 인화점
- 25 °F · −25 °F
- 저장 조건
- -20 °C · -20°C
- 용해도
- 물과 반응
- 물리적 상태
- 액체
- Specific Gravity
- 1.47 · 1.47
- 색상
- 무색~붉은색 투명
- 수용성
- 물과 반응
- BRN
- 1731136 · 1731136
- 안정성
- Moisture Sensitive (Reactive)
- InChI
- 1S/C3H9ISi/c1-5(2,3)4/h1-3H3
- InChIKey
- CSRZQMIRAZTJOY-UHFFFAOYSA-N
- SMILES
- C[Si](C)(C)I
- NIST
- Iodotrimethylsilane(16029-98-4)
- EPA
- Silane, iodotrimethyl- (16029-98-4)
화학적 성질
Straw liquid
안전 및 규제
GHS 분류
GHS Classification
Danger
H225 (98.4%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P321, P363, P370+P378, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 62 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
Regulatory Information
Chemical: Silane, iodotrimethyl-
Status: Active Update: 23-11-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/24465
Iodotrimethylsilane: Does not have an individual approval but may be used under an appropriate group standard
독성 정보
안전 데이터
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 2924 3/PG 2
- HS 번호
- 29310095
- risk_code
- 11-14-34
- hazard_code
- F,C
- safety_code
- 16-26-36/37/39-43-45-25
- 포장분류
- II
- 위험 등급
- 3
- 기존화학 물질
- KE-21044
- F 고인화성물질
- 8-21
- Hazard Classifications
- Eye Dam. 1Flam. Liq. 2Skin Corr. 1B
- 스토리지 클래스
- 3 - Flammable liquids
화학 및 산업
용도 및 제조
응용 분야
용도Iodotrimethylsilane is used for the introduction of trimethylsilyl group in organic synthesis. It is also useful for gas chromatography analysis by converting alcohol into a silyl ether derivative, thereby making it more volatile than the original molecule.Iodotrimethylsilane is a highly efficient reagent for the cleavage of ethers, esters, carbamates, ketals, and lactones. It is also used for the introduction of TMS groups, such as TMS enol ethers, and is a key reagent for the selective removal of N-Cbz groups in the presence of a trimethyltin moiety.This reagent has recently been reported to convert allyl and benzyl phosphotriesters to the corresponding iodides.
일반 설명Iodotrimethylsilane is a multipurpose reagent used in various organic reactions. It is used for the dealkylation of few compounds like lactones, ethers, acetals, and carbamates and trimethylsilylating agent for the synthesis of silyl imino esters, alkyl and alkenyl silanes, etc. It also acts as a Lewis acid catalyst and as a reducing agent in many organic reactions.
제조 방법
Iodotrimethylsilane is prepared by mixing equimolar amounts of chlorotrimethylsilane and sodium iodide in acetonitrile, reduces various benzylic alcohols to the corresponding phenylalkanes. Other have been reported for the preparation of Trimethylsilyl Iodide(TMS-I): chlorotrimethylsilane undergoes halogen exchange with either lithium iodide in CHCl3 or sodium iodide in MeCN, which allows in situ reagent formation. Alternatively, hexamethyldisilane reacts with iodine at 25–61°C to afford TMS-I with no byproducts.
상·하류 제품 정보
상류 원료
하류 제품
공급사50 곳
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