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18817-29-3

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18817-29-3 Usage

General Description

5-Hexenyltrichlorosilane is a synthetic, odorless chemical compound represented by the formula C6H11SiCl3. It belongs to the class of organosilicon compounds, characterized by a carbon-silicon bond. The designation 'trichlorosilane' signifies that three chlorine atoms are attached to the silicon atom, while '5-Hexenyl' indicates a six-carbon chain with a double bond located on the fifth carbon. This substance is generally used in the field of organic synthesis or as a precursor to more complex chemicals. Its physical properties, health hazards, or environmental impact remain less understood, thus warranting precaution while handling and storing.

Check Digit Verification of cas no

The CAS Registry Mumber 18817-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18817-29:
(7*1)+(6*8)+(5*8)+(4*1)+(3*7)+(2*2)+(1*9)=133
133 % 10 = 3
So 18817-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11Cl3Si/c1-2-3-4-5-6-10(7,8)9/h2H,1,3-6H2

18817-29-3SDS

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 trichloro(hex-5-enyl)silane

1.2 Other means of identification

Product number -
Other names 5-HEXENYLTRICHLOROSILANE

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:18817-29-3 SDS

18817-29-3Relevant articles and documents

Effect of ether on regioselectivity in hydrosilylation of 1,5-hexadiene with chlorohydrosilanes catalyzed by homogeneous platinum catalysts

Saiki, Takeaki

experimental part, p. 1556 - 1563 (2009/10/14)

Hydrosilylation of 1,5-hexadiene with chlorohydrosilanes catalyzed by homogeneous platinum catalyst to produce 5-hexenylchlorosilanes was studied. The presence of ether additives was highly effective in improving the regioselectivity and the yield. The formation of a double-bond rearrangement isomer, cis-, or trans-4-hexenylchlorosilanes, during the hydrosilylation was reduced drastically, as well. Copyright Taylor & Francis Group, LLC.

Alkenylsilane effects on organotitanium-catalyzed ethylene polymerization. Toward simultaneous polyolefin branch and functional group introduction

Amin, Smruti B.,Marks, Tobin J.

, p. 4506 - 4507 (2007/10/03)

The comonomer 5-hexenylsilane is introduced into organotitanium-mediated ethylene polymerizations to produce silane-terminated ethylene/5-hexenylsilane copolymers. The resulting polymers were characterized by 1H and 13C NMR, GPC, and DSC. High activities (up to 107 g polymer/(mol Ti·atm ethylene·h)) and narrow polydispersities are observed in the polymerization/chain transfer process. Ethylene/5-hexenylsilane copolymer molecular weights are found to be inversely proportional to 5-hexenylsilane concentration, supporting a silanolytic chain transfer mechanism. Control experiments indicate that chain transfer mechanism by 5-hexenylsilane is significantly more efficient than that of n-hexylsilane for organotitanium-mediated ethylene polymerization. The present study represents the first case in which a functionalized comonomer is efficiently used to effect both propagation and chain transfer chemistry during olefin polymerization. Copyright

Method for controlling hydrosilylation in a reaction mixture

-

, (2008/06/13)

This invention discloses a method of controlling hydrosilylations in a reaction mixture by controlling the solution concentration of oxygen in the reaction mixture, relative to any platinum present in the reaction mixture. This invention further discloses a method for controlling isomerization in linear or branched alkenyl compounds having at least 4 carbon atoms during a hydrosilylation reaction by introducing a controlled amount of oxygen into the alkenyl compounds during the hydrosilylation. This invention further discloses a method for producing dicycloalkylsubstituted silanes by reacting a halo-or alkoxy-silane with a unsaturated cycloalkenyl compound in the presence of oxygen and a hydrosilylation catalyst.

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