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17903-46-7

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17903-46-7 Usage

Description

(Chloromethyl)(4-methoxyphenyl)dimethylsilane is a versatile silane compound that features a chloromethyl group, a 4-methoxyphenyl group, and two dimethylsilane groups. It serves as a valuable building block in organic synthesis, particularly for the incorporation of the 4-methoxyphenyl group into a range of organic molecules. This chemical is widely recognized for its utility in the synthesis of pharmaceuticals, agrochemicals, and materials science, while its silane functionality positions it as a key precursor for silicon-based polymers and materials development.

Uses

Used in Pharmaceutical Synthesis:
(Chloromethyl)(4-methoxyphenyl)dimethylsilane is used as a synthetic building block for the creation of various pharmaceutical compounds. Its unique structure allows for the efficient introduction of the 4-methoxyphenyl group into drug molecules, potentially enhancing their therapeutic properties and efficacy.
Used in Agrochemical Development:
In the agrochemical industry, (chloromethyl)(4-methoxyphenyl)dimethylsilane is utilized as a reagent for the synthesis of novel agrochemicals. The 4-methoxyphenyl group's incorporation can lead to the development of more effective and targeted pest control agents, contributing to improved crop protection strategies.
Used in Materials Science:
(Chloromethyl)(4-methoxyphenyl)dimethylsilane is employed as a key component in the development of advanced materials. Its silane functionality makes it an ideal precursor for the synthesis of silicon-based polymers and materials, which can be applied in various high-tech industries, including electronics, aerospace, and automotive.
Used in Silicon-based Polymers and Materials Preparation:
Within the field of materials science, (chloromethyl)(4-methoxyphenyl)dimethylsilane is used as a precursor for the preparation of silicon-based polymers and materials. Its unique structure facilitates the creation of new materials with enhanced properties, such as improved thermal stability, mechanical strength, and chemical resistance, suitable for a range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17903-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17903-46:
(7*1)+(6*7)+(5*9)+(4*0)+(3*3)+(2*4)+(1*6)=117
117 % 10 = 7
So 17903-46-7 is a valid CAS Registry Number.

17903-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4-methoxyphenyl)dimethylsilyl]methyl chloride

1.2 Other means of identification

Product number -
Other names chloromethyldimethyl(4-methoxyphenyl)silane

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:17903-46-7 SDS

17903-46-7Relevant articles and documents

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Eaborn,Jeffrey

, p. 4266 (1954)

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A novel method for preparing silanols from silylmethanols

Takeda, Daisuke,Oyama, Ryo,Yamada, Shozo

supporting information; experimental part, p. 532 - 533 (2011/04/22)

Various types of silylmethanols were converted into their corresponding silanols in good to excellent yield under mild oxidation conditions using TEMPO (2,2,6,6-tetramethyl-l-piperidinyloxyl). Copyright

Fungicidal (1H-1,2,4-triazolyl)disilaalkanes

-

, (2008/06/13)

This invention relates to (1H-1,2,4-triazolyl)disilaalkanes as represented by formula I, their preparation, and their use in controlling fungus diseases of living plants. STR1 wherein R1, R2, R3, R4, and R5 can be independently lower alkyl, vinyl, allyl, benzyl, or substituted phenyl such as para-fluorophenyl, para-chlorophenyl, para-enthoxyphenyl, and biphenyl.

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