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Hexyl(trimethyl)silane, also known as hexyltrimethylsilane, is an organosilicon compound with the chemical formula C9H22Si. It is a colorless liquid at room temperature and is derived from the combination of a hexyl group (C6H13) and a trimethylsilyl group (Si(CH3)3). hexyl(trimethyl)silane is primarily used as a reagent in organic synthesis, particularly in the formation of silyl ethers and as a protecting group for alcohols. It is also employed as a coupling agent in the production of silicone-based materials and as a surfactant in various industrial applications. Due to its stability and reactivity, hexyl(trimethyl)silane plays a significant role in the field of organosilicon chemistry.

3429-62-7

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3429-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3429-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3429-62:
(6*3)+(5*4)+(4*2)+(3*9)+(2*6)+(1*2)=87
87 % 10 = 7
So 3429-62-7 is a valid CAS Registry Number.

3429-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hexyl(trimethyl)silane

1.2 Other means of identification

Product number -
Other names 1-Hexyl-trimethylsilan

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:3429-62-7 SDS

3429-62-7Downstream Products

3429-62-7Relevant academic research and scientific papers

Ga+-catalyzed hydrosilylation? about the surprising system Ga+/HSiR3/olefin, proof of oxidation with subvalent Ga+and silylium catalysis with perfluoroalkoxyaluminate anions

Barthélemy, Antoine,Glootz, Kim,Hanske, Annaleah,Krossing, Ingo,Scherer, Harald

, p. 439 - 453 (2022/01/22)

Already 1 mol% of subvalent [Ga(PhF)2]+[pf]- ([pf]- = [Al(ORF)4]-, RF = C(CF3)3) initiates the hydrosilylation of olefinic double bonds under mild conditions. Reactions with HSiMe3 and HSiEt3 as substrates efficiently yield anti-Markovnikov and anti-addit

Synthesis of (E)-alkenes via hydroindation of C{triple bond, long}C in InCl3-NaBH4 system

Wang, Chunyan,Yan, Lei,Zheng, Zhiguo,Yang, Deyu,Pan, Yuanjiang

, p. 7712 - 7717 (2007/10/03)

In InCl3-NaBH4-MeCN system, terminal aryl alkynes could couple with aryl iodides and bromides to give disubstituted alkenes via hydroindation of C{triple bond, long}C. In the similar way, (E)-alkenylsilanes were synthesized via reduction of alkynylsilanes in tetrahydrofuran (THF) in high yields. The processes showed high regio- and stereoselectivity.

REGIOCONTROLLED SYNTHESIS OF ALLYLSILANES BY MEANS OF RHODIUM(I) OR IRIDIUM(I) CATALYZED ISOMERIZATION OF OLEFINS

Matsuda, Isamu,Kato, Tomohisa,Sato, Susumu,Izumi, Yusuke

, p. 5747 - 5750 (2007/10/02)

Rhodium(I) or iridium(I) catalyzed migration of double-bond has been successfully applied to the regiocontrolled synthesis of allylsilane from olefin silylated at a remote sp3 carbon.

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