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Propanoic acid, 2-methyl-3-(trichlorosilyl)-, methyl ester is a complex organic compound with the chemical formula C6H11Cl3O2Si. It is a derivative of propanoic acid, featuring a methyl group at the 2nd carbon and a trichlorosilyl group at the 3rd carbon. The trichlorosilyl group consists of a silicon atom bonded to three chlorine atoms. Propanoic acid, 2-methyl-3-(trichlorosilyl)-, methyl ester is an ester, formed by the reaction of propanoic acid with methanol, where the hydroxyl group of the acid is replaced by a methyl group. It is used in various chemical processes and applications, particularly in the synthesis of organosilicon compounds and as a precursor in the production of silicone materials. Due to its reactivity and the presence of the trichlorosilyl group, it is important to handle Propanoic acid, 2-methyl-3-(trichlorosilyl)-, methyl ester with care, following appropriate safety protocols.

3451-82-9

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3451-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3451-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3451-82:
(6*3)+(5*4)+(4*5)+(3*1)+(2*8)+(1*2)=79
79 % 10 = 9
So 3451-82-9 is a valid CAS Registry Number.

3451-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-methyl-3-trichlorosilylpropanoate

1.2 Other means of identification

Product number -
Other names methyl 2-methyl-3-trichlorosilylpropionate

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:3451-82-9 SDS

3451-82-9Downstream Products

3451-82-9Relevant academic research and scientific papers

Homogeneous catalytic hydrosilylation of the C=C double bond in the presence of transition metal catalysts

Skoda-Foeldes, Rita,Kollar, Laszlo,Heil, Balint

, p. 297 - 304 (2007/10/02)

Hydrosilylation of unsaturated esters and other vinyl- and vinylidene type olefins has been carried out with PtCl2(PhCN)2, RhCl(PPh3)3 and platinum-phosphine catalysts.With PtCl2(PhCN)2 and platinum(0)-phosphine complexes as catalysts the hydrosilylation of methyl methacrylate gave the linear product 2a, whereas in the RhCl(PPh3)-catalyzed reaction the silyl ketene acetal derivative 4a was formed selectively.In the reactions of other esters and unsaturated hydrocarbons the main product is highly dependent on the structure of the substrate, but the catalyst used is also very important.With unsaturated hydrocarbons the selectivity is rather poor, but in the case of 1-vinyl-2-pyrrolidinone the linear- (9e) and the branched hydrosilylated derivative (10e) are formed in high yields depending on the catalyst used.The platinum(II)-phosphine complexes are inactive in the absence of air, but some platinum(0)-phosphine catalysts are also effective under argon in the hydrosilylation of methyl methacrylate.

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