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18387-98-9

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18387-98-9 Usage

General Description

3-Acetoxypropyl dimethylchlorosilane is a chemical compound with the molecular formula C7H15ClO2Si. It is a colorless liquid with a strong odor and is commonly used as a coupling agent and surface modifier in various industrial applications. 3-Acetoxypropyl dimethylchlorosilane is highly reactive and can be used in the manufacturing of adhesives, sealants, and coatings. It is also used as a silane coupling agent to improve the adhesion between organic polymers and inorganic materials such as glass, metal, and ceramics. Additionally, it is used in the production of silicone polymers and resins, and as a crosslinking agent in the manufacturing of silicone rubber. However, it is important to handle this chemical with caution as it is highly flammable and can cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 18387-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18387-98:
(7*1)+(6*8)+(5*3)+(4*8)+(3*7)+(2*9)+(1*8)=149
149 % 10 = 9
So 18387-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H15ClO2Si/c1-7(9)10-5-4-6-11(2,3)8/h4-6H2,1-3H3

18387-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[chloro(dimethyl)silyl]propyl acetate

1.2 Other means of identification

Product number -
Other names (3-Acetoxy-propyl)-chlor-dimethyl-silan

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:18387-98-9 SDS

18387-98-9Relevant articles and documents

PROCESS FOR SYNTHESIS OF ORGANOSILICON COMPOUNDS FROM HALOSILANES

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Paragraph 0150-0151, (2022/02/09)

A process for synthesis of an organosilicon compound is provided herein. Also, novel organosilicon compounds prepared by the present process is provided herein. The process comprises the reaction of a halosilane with an organofunctional alkyl halide in the presence of a metal catalyst, a promoter, and an optional co-catalyst. The process provides an efficient synthetic route to produce organosilicon compounds. The process also allows synthesis of organosilicon compounds with a plurality of different functional groups.

Method for preparing hydroxyalkyl disiloxane

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Paragraph 0049; 0050; 0051; 0052; 0053; 0054; 0087, (2017/07/22)

The invention relates to a method for preparing hydroxyalkyl disiloxane. The method includes the following steps: (1) mixing carboxylic acid unsaturated ester with dimethylchlorosilane in an organic solvent, introducing inert gas, adding hydrosilyation catalyst and stirring for 2 to 12 hours; (2) dropwising a mixed liquid of acidic aqueous solution and the organic solvent to the hydrosilylation reaction product and hydrolyzing for 1 to 6 hours; (3) regulating the hydrolysis product pH to be neutral, extracting organic layers three times with extraction agent, washing three times, drying for 24 hours and removing the extraction agent by rotary evaporating to obtain the finished product. The method has the advantages of simple operation, simple steps, mild reaction conditions, pure product and high yield, and the yield of the hydrosilylation reaction product can reach 83.2% and the yield of the hydrolysis product can reach 89.5%.

Mechanistic insights into the hydrosilylation of allyl compounds - Evidence for different coexisting reaction pathways

Gigler, Peter,Drees, Markus,Riener, Korbinian,Bechlars, Bettina,Herrmann, Wolfgang A.,Kuehn, Fritz E.

, p. 1 - 14 (2013/01/14)

The hydrosilylation of allyl compounds is often accompanied by the formation of high amounts of byproducts. The formation processes have not been fully understood so far. In this work, the allyl hydrosilylation mechanism is investigated in detail and experimental and theoretical evidence for multiple, coexisting reaction pathways is provided. Based on earlier reports and the observations during an extensive catalytic study, different pathways, leading to the observed byproducts, were identified and proven by labeling experiments and DFT calculations. Oxidative addition of the silane and the insertion of the allyl compound into the Pt-H bond turned out to be the crucial, selectivity-determining steps within the catalytic cycle. Based on these findings, it should be possible to systematically influence these steps and pave the way to a rational and straightforward design of more selective catalysts.

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