95541
三甲基氯硅烷
Wacker Chemie AG, ≥99.0% (GC)
别名:
硅烷 M3, TMCS, Trimethylchlorosilane, 三甲基硅基氯
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关于此项目
线性分子式:
(CH3)3SiCl
化学文摘社编号:
分子量:
108.64
UNSPSC Code:
12352302
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-900-5
Beilstein/REAXYS Number:
1209232
MDL number:
产品名称
三甲基氯硅烷, Wacker Chemie AG, ≥99.0% (GC)
InChI key
IJOOHPMOJXWVHK-UHFFFAOYSA-N
InChI
1S/C3H9ClSi/c1-5(2,3)4/h1-3H3
SMILES string
C[Si](C)(C)Cl
vapor density
3.7 (vs air)
vapor pressure
100 mmHg ( 25 °C)
assay
≥99.0% (GC)
form
liquid
autoignition temp.
752 °F
expl. lim.
6.4 %
manufacturer/tradename
Wacker Chemie AG
refractive index
n20/D 1.387 (lit.)
bp
57 °C (lit.)
mp
−40 °C (lit.)
density
0.856 g/mL at 25 °C (lit.)
Quality Level
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Application
氯三甲基硅烷的可能用途：
它也用于 Fisher 糖基化。
- 聚砜 (PSU) 的氯甲基化。
- 活化氢化锂，将其转化为氢化物源，用于羰基化合物的还原硅烷化。
- 三甲基氯硅烷/溴化锂形成了一种有效的醇转化为溴化物的试剂。
- 氯三甲基硅烷在钐促进的烯丙基和 α-环丙烷化中活化作用是氯化汞的无毒替代物-烯醇。
它也用于 Fisher 糖基化。
General description
三甲基氯硅烷是一种氯-有机硅烷化合物，主要用于甲硅烷基化反应。
Other Notes
根据要求提供批量采购价
硅烷 M3
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-18.4 °F - closed cup
flash_point_c
-28 °C - closed cup
ppe
Faceshields, Gloves, Goggles
法规信息
危险化学品
此项目有
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 4, 1060-1060 (2014)
A practical method for activation of commercial lithium hydride: reductive silylation of carbonyl compounds with lithium hydride and chlorotrimethylsilane.
Ohkuma T, et al.
The Journal of Organic Chemistry, 59(1), 217-221 (1994)
Modification of polysulfones by click chemistry: amphiphilic graft copolymers and their protein adsorption and cell adhesion properties.
Yilmaz G, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 49(1), 110-117 (2011)
Chlorotrimethylsilane as an Activating Reagent in the Samarium-Promoted Cyclopropanation of Allylic and ?-Allenic Alcohols.
Lautens M
The Journal of Organic Chemistry, 61(6), 2210-2214 (1996)
Chlorotrimethylsilane/lithium bromide and hexamethyldisilane/pyridinium bromide perbromide: effective and selective reagents for the conversion of alkyl (cycloalkyl and aralkyl) alcohols into bromides.
Olah GA, et al.
The Journal of Organic Chemistry, 45(9), 1638-1639 (1980)
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