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10605-40-0

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10605-40-0 Usage

Uses

Chloro(3-chloropropyl)dimethylsilane can be used as:A starting material to prepare misonidazole-based 18F-radiolabeled organosilicon compounds as positron emission tomography (PET) ligands for medical imaging applications.An intermediate in the synthesis of block copolymers.

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.

A General and Selective Synthesis of Methylmonochlorosilanes from Di-, Tri-, and Tetrachlorosilanes

Naganawa, Yuki,Nakajima, Yumiko,Sakamoto, Kei

supporting information, p. 601 - 606 (2021/01/13)

Direct catalytic transformation of chlorosilanes into organosilicon compounds remains challenging due to difficulty in cleaving the strong Si-Cl bond(s). We herein report the palladium-catalyzed cross-coupling reaction of chlorosilanes with organoaluminum reagents. A combination of [Pd(C3H5)Cl]2 and DavePhos ligand catalyzed the selective methylation of various dichlorosilanes 1, trichlorosilanes 5, and tetrachlorosilane 6 to give the corresponding monochlorosilanes.

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.

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