요오드트리메틸실란

Trimethylsilyl iodide

HCID 85247CAS 16029-98-4

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

Iodotrimethylsilane16029-98-4TrimethyliodosilaneTrimethylsilyl iodideiodo(trimethyl)silaneSilane, iodotrimethyl-7A65KRZ6NVMe3SiIDTXSID4065997TMSI cpdRefChem:148569DTXCID5035161
이름 더 보기
요오드트리메틸실란요오드트리메틸실란(IODOTRIMETHYLSILANE)TMS iodideCT3610IodotrimethyLTrimethylsilyl ioIodotrmethylsilanetrimethyiodosilaneCo-Formula CFS-710
240-171-0TMSIMFCD00001028Iodotrimethylsilane (>90%)TMISIodotrimethylsilane; TMSI;Trimethylsilicon iodide; Trimethylsilyl iodidetrimethylsilyliodideC3H9ISi

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

실험 및 물리화학적 성질

Chemical ClassesMetals -> Metalloid Compounds (Silicon)
SpringerMaterials Properties29Si nuclear magnetic resonance spectrum
Physical DescriptionClear light brown liquid; [Sigma-Aldrich MSDS]

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

화학적 성질

Straw liquid

안전 및 규제

GHS 분류

GHS Classification · 4건

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 · 3건

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

Hazards SummaryReacts violently with water; Causes burns; Inhalation may cause corrosive injuries to upper respiratory tract and lungs; [Sigma-Aldrich MSDS] See Silicon tetraiodide.
Hazard Classes and CategoriesFlam. Liq. 2 (98.4%)

독성 정보

Adverse EffectsDermatotoxin - Skin burns.

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

화학 및 산업

용도 및 제조

UsesUsed as an intermediate; [ExPub: ECHA REACH Registrations]
General Manufacturing InformationSilane, iodotrimethyl-: ACTIVE
응용 분야 · 2건

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 · 1건

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.

공급사50 곳

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