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Methyl 3-(dichloromethylsilyl)-2-methylpropionate is a chemical compound with the molecular formula C6H12Cl2O2Si. It is an organosilicon compound, which means it contains silicon along with carbon, hydrogen, and oxygen atoms. This specific compound features a methyl ester group (CH3-COO-) attached to a 2-methylpropionate (isobutyrate) backbone, with a dichloromethylsilyl group (Si(CH2Cl2)-) substituting one of the carbon atoms in the isobutyrate chain. The dichloromethylsilyl group is of interest due to its potential applications in organic synthesis, particularly as a protecting group or in the formation of carbon-carbon bonds. The compound's structure and reactivity make it a valuable intermediate in the synthesis of more complex organic molecules, especially in the field of pharmaceuticals and materials science.

4074-06-0

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4074-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4074-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4074-06:
(6*4)+(5*0)+(4*7)+(3*4)+(2*0)+(1*6)=70
70 % 10 = 0
So 4074-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Cl2O2Si/c1-5(6(9)10-2)4-11(3,7)8/h5H,4H2,1-3H3

4074-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name β-(dichloro-methyl-silanyl)-isobutyric acid methyl ester

1.2 Other means of identification

Product number -
Other names β-(Dichlor-methyl-silyl)-isobuttersaeure-methylester

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:4074-06-0 SDS

4074-06-0Relevant academic research and scientific papers

A magnetically recyclable superparamagnetic silica supported Pt nanocatalyst through a multi-carboxyl linker: Synthesis, characterization, and applications in alkene hydrosilylation

Li, Laiming,Li, Youxin,Yan, Jincong,Cao, Hang,Shao, Dongyun,Bao, James J.

, p. 12696 - 12709 (2019/05/06)

To simplify separation procedures, improve the reusability and decrease the loss of Pt, two Pt catalysts anchored on superparamagnetic silica (Fe3O4@SiO2-EDTA@Pt and Fe3O4@SiO2-DTPA@Pt) were prepared for the first time. The stable magnetic properties made them easily recyclable using a magnet rather than filtration, decantation or centrifugation. After 12 catalytic runs for both 30-50 nm Pt catalysts, the yield of 1-heptylmethyldichlorosilane was still up to 90%. The average loss of Pt in each reaction was only 0.87% for Fe3O4@SiO2-EDTA@Pt and 0.66% for Fe3O4@SiO2-DTPA@Pt owing to the strong interaction between Pt and carboxyl. The unprecedented activity and selectivity of the two Pt nanoparticle catalysts were observed in the hydrosilylation of alkenes. The turnover number in the reaction between 1-hexene and methyldichlorosilane using 5 × 10-8 mol of the Pt approached 662733 for Fe3O4@SiO2-EDTA@Pt and 579947 for Fe3O4@SiO2-DTPA@Pt over 12 h. The corresponding hydrosilylation products in excellent yields were obtained when we employed a broad range of alkenes as substrates, including 5 isomerous hexenes and 14 important industry raw materials. Fe3O4@SiO2-DTPA@Pt showed a better activity. They have potential for catalyzing more reactions and replacing the current homogeneous Pt catalysts in industry.

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