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About This Item
线性分子式:
[(CH3)3Si]2CHCl
CAS号:
分子量:
194.85
Beilstein:
1736681
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
97%
形式
liquid
折射率
n20/D 1.449 (lit.)
bp
57-60 °C/15 mmHg (lit.)
密度
0.892 g/mL at 25 °C (lit.)
SMILES字符串
C[Si](C)(C)C(Cl)[Si](C)(C)C
InChI
1S/C7H19ClSi2/c1-9(2,3)7(8)10(4,5)6/h7H,1-6H3
InChI key
XNJGZHVYPBNLEB-UHFFFAOYSA-N
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应用
Chlorobis(trimethylsilyl)methane can be used as a reagent for the preparation of:
- Para-bis(trimethylsilyl)ethylstyrene (PBTES) monomer, which is used to synthesize corresponding network polymer of styrene.
- Bis(trimethylsilyl)methyl magnesium chloride (Grignard reagent), which is used in the synthesis of bis(trimethylsilyl) allyl compounds by reacting with alkenyl bromide via the Kumada coupling reaction.
- N-[Bis(trimethylsilyl)methyl]heterocumulenes.
警示用语：
Warning
危险分类
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
118.4 °F - closed cup
闪点(°C)
48 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Synthesis and Reactivity of N-[Bis (trimethylsilyl) methyl] heterocumulenes
Barbaro G, et al.
The Journal of Organic Chemistry, 60(19), 6032-6039 (1995)
David R Williams et al.
Organic letters, 8(20), 4393-4396 (2006-09-22)
Allylation reagents, which possess geminal bis-trimethylsilyl substitution, are readily prepared from E- or Z-alkenyl bromides. The reactivity of 3,3-bis(trimethylsilyl)-2-methyl-1-propene (1) is described and predominantly provides ene reactions with aldehydes to give alcohol 2 in the presence of BF3.OEt2. Alternatively, Sakurai
Synthesis of some silyl mono-and polystyrenes with new properties
Assadi, MG and Hosseinzadeh, F
Designed Monomers and Polymers, 13(2), 181-191 (2010)
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