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18236-89-0

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18236-89-0 Usage

Chemical Properties

clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 18236-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18236-89:
(7*1)+(6*8)+(5*2)+(4*3)+(3*6)+(2*8)+(1*9)=120
120 % 10 = 0
So 18236-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H10Cl2Si/c1-4(2)7(3,5)6/h4H,1-3H3

18236-89-0SDS

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 dichloro-methyl-propan-2-ylsilane

1.2 Other means of identification

Product number -
Other names Silane, dichloromethyl(1-methylethyl)-

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:18236-89-0 SDS

18236-89-0Downstream Products

18236-89-0Relevant articles and documents

Quantitative substituent effects in the Grignard reaction with silanes

Golubev, Oleg,Panov, Dmitri,Ploom, Anu,Tuulmets, Ants,Nguyen, Binh T.

, p. 3700 - 3705 (2008/02/08)

Kinetics of reactions of ethyl- and phenylmagnesium chlorides with chlorosilanes, RMeSiCl2, were investigated in diethyl ether under pseudo-first order conditions with a great excess of the Grignard reagent. Rate constants for alkyl substituted silanes correlate well with Es(Si) steric parameters. A good linear correlation of rate data for substituted phenyl derivates with σ0 inductive constants together with correlations of the literature data rule out the resonance effect of substituents at least in nucleophilic displacement reactions at the silicon center. An attempt to calculate the steric constants for polar substituents was made. It appeared that the inductive constants σ* derived from the carbon chemistry are not applicable to the silicon chemistry. New scales of parameters for description of polar and steric effects in the organosilicon chemistry need to be created.

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