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18171-30-7

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18171-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18171-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18171-30:
(7*1)+(6*8)+(5*1)+(4*7)+(3*1)+(2*3)+(1*0)=97
97 % 10 = 7
So 18171-30-7 is a valid CAS Registry Number.

18171-30-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-dimethyl-(trichloromethyl)silane

1.2 Other means of identification

Product number -
Other names Dimethyl-trichlormethyl-chlorsilan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18171-30-7 SDS

18171-30-7Downstream Products

18171-30-7Relevant articles and documents

Complexation of paramagnetic intermediates formed in the photolysis of 7,7-dimethyl-1,4,5,6-tetraphenyl-2,3-benzo-7-silanorbornadiene: A study by spin chemistry methods

Leshina,Taraban,Plyusnin,Volkova,Egorov

, p. 421 - 426 (2000)

Complexation of paramagnetic intermediates formed in the photolysis of 7,7-dimethyl-1,4,5,6-tetraphenyl-2,3-benzo-7-silanorbornadiene with n-donors (PPh3, O2) was studied by spin chemistry methods.

CONVERSION OF DISILANES TO FUNCTIONAL MONOSILANES XIV. REACTIONS OF METHYLCHLORODISILANES WITH gem-POLYHALIDES CATALYZED BY ORGANIC BASES

Matsumoto, Hideyuki,Ohkawa, Kazuhiro,Matsubara, Ikuya,Kasahara, Miyuki,Arai, Takeshi,Nagai, Yoichiro

, p. 29 - 38 (2007/10/02)

The reaction of methylchlorodisilanes with gem-polyhalides in the presence of organic bases has been investigated.The compounds CXCl2SiMeCl2 (X = Cl, H, F and SiMeCl2) were obtained in moderate to high yields from Cl2MeSiSiMeCl2 and polyhalomethanes (e.g., CCl4, CHCl3, CFCl3 and CCl3SiMeCl2) with PPh3 or Bu4NCl as catalyst.The reaction of 1,1,2-trichlorotrimethyldisilane with CCl4 afforded a 1:1 mixture of CCl3SiMeCl2 and CCl3SiMe2Cl.Also, XC6H4CCl2SiMeCl2 (X = H and 4-Cl) were obtained in moderate yields from Cl2MeSiSiMeCl2 and XC6H4CCl3 with Bu4NCl or Bu4NF as catalyst.

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