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10605-40-0

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10605-40-0 Usage

Description

3-Chloropropyldimethylchlorosilane is an organosilicon compound characterized by its chloropropyl and dimethylchlorosilane functional groups. It is a versatile chemical intermediate with potential applications in various industries due to its unique chemical properties.

Uses

Used in Medical Imaging Applications:
3-Chloropropyldimethylchlorosilane is used as a starting material for the preparation of misonidazole-based 18F-radiolabeled organosilicon compounds. These compounds serve as positron emission tomography (PET) ligands, which are essential in medical imaging for diagnosing and monitoring various diseases, particularly cancer.
Used in Polymer Synthesis:
3-Chloropropyldimethylchlorosilane is also utilized as an intermediate in the synthesis of block copolymers. Block copolymers are materials composed of two or more covalently bonded polymer chains with different structures, which can exhibit unique properties and be tailored for specific applications in various industries, such as pharmaceuticals, materials science, and engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 10605-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,6,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10605-40:
(7*1)+(6*0)+(5*6)+(4*0)+(3*5)+(2*4)+(1*0)=60
60 % 10 = 0
So 10605-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H12Cl2Si/c1-8(2,7)5-3-4-6/h3-5H2,1-2H3

10605-40-0 Well-known Company Product Price

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  • Aldrich

  • (26230)  Chloro(3-chloropropyl)dimethylsilane  technical, ≥95% (GC)

  • 10605-40-0

  • 26230-10ML

  • 4,095.00CNY

  • Detail

10605-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-(3-chloropropyl)-dimethylsilane

1.2 Other means of identification

Product number -
Other names Chloro(3-chloropropyl)dimethylsilane

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:10605-40-0 SDS

10605-40-0Relevant articles and documents

Functionalization on silica gel with allylsilanes. A new method of covalent attachment of organic functional groups on silica gel

Shimada, Toyoshi,Aoki, Kazuko,Shinoda, Yo,Nakamura, Tomoaki,Tokunaga, Norihito,Inagaki, Shinji,Hayashi, Tamio

, p. 4688 - 4689 (2003)

Treatment of an (allyl)organosilane with silica gel in refluxing toluene brought about deallylation forming an Si-O-Si bond with the silicon on the silica gel. This Si-O-Si bond formation provides us with a new reliable method for the functionalization of a silica gel surface. Copyright

Surface functionalization of silica by Si-H activation of hydrosilanes

Moitra, Nirmalya,Ichii, Shun,Kamei, Toshiyuki,Kanamori, Kazuyoshi,Zhu, Yang,Takeda, Kazuyuki,Nakanishi, Kazuki,Shimada, Toyoshi

, p. 11570 - 11573 (2014)

Inspired by homogeneous borane catalysts that promote Si-H bond activation, we herein describe an innovative method for surface modification of silica using hydrosilanes as the modification precursor and tris(pentafluorophenyl) borane (B(C6F5)3) as the catalyst. Since the surface modification reaction between surface silanol and hydrosilane is dehydrogenative, progress and termination of the reaction can easily be confirmed by the naked eye. This new metal-free process can be performed at room temperature and requires less than 5 min to complete. Hydrosilanes bearing a range of functional groups, including alcohols and carboxylic acids, have been immobilized by this method. An excellent preservation of delicate functional groups, which are otherwise decomposed in other methods, makes this methodology appealing for versatile applications.

PROCESS FOR PRODUCING DIMETHYLCHLOROSILANE COMPOUND

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Paragraph 0090-0091; 0095, (2021/11/20)

A process for producing a dimethylchlorosilane compound of formula (2) below: wherein X represents a halogen atom or an acyloxy group having 2 to 20 carbon atoms, the process including the step of: reacting an allyl compound of formula (1) below: wherein X has a meaning same as above, with dimethylchlorosilane in presence of an iridium catalyst,wherein the dimethylchlorosilane has a content of 1,1,3,3-tetramethyldisiloxane of 5.0 wt % or less.

Production of dimethylchlorosilane

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Paragraph 0037-0040; 0042, (2021/11/19)

A process for producing a dimethylchlorosilane compound of formula (2) below:wherein X represents a halogen atom or an acyloxy group having 2 to 20 carbon atoms,the process including the step of:reacting an allyl compound of formula (1) below:wherein X has a meaning same as above,with dimethylchlorosilane in presence of an iridium catalyst,wherein the dimethylchlorosilane has a content of 1,1,3,3-tetramethyldisiloxane of 5.0 wt% or less.

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