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Trisiloxane, 1,1,1,3,5,5,5-heptamethyl-3-(2-propenyl)-, also known as 1,1,1,3,5,5,5-heptamethyltrisiloxane-3-allyl, is a cyclic organosilicon compound with the chemical formula C9H24O2Si3. It consists of a trisiloxane ring with three silicon atoms, each connected to an oxygen atom, and seven methyl groups attached to the silicon atoms. The compound also features an allyl group (2-propenyl) attached to one of the silicon atoms, which provides a reactive site for further chemical modifications. Trisiloxane, 1,1,1,3,5,5,5-heptamethyl-3-(2-propenyl)- is used in various applications, such as in the production of silicone-based polymers, as a coupling agent in composite materials, and as a component in specialty coatings and adhesives. Its unique structure and properties make it valuable in the field of materials science and chemical engineering.

7087-20-9

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7087-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7087-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7087-20:
(6*7)+(5*0)+(4*8)+(3*7)+(2*2)+(1*0)=99
99 % 10 = 9
So 7087-20-9 is a valid CAS Registry Number.

7087-20-9SDS

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 trimethyl-(methyl-prop-2-enyl-trimethylsilyloxysilyl)oxysilane

1.2 Other means of identification

Product number -
Other names 3-Allyl-heptamethyl-trisiloxan

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:7087-20-9 SDS

7087-20-9Downstream Products

7087-20-9Relevant academic research and scientific papers

Bis(imino)pyridine cobalt-catalyzed dehydrogenative silylation of alkenes: Scope, mechanism, and origins of selective allylsilane formation

Atienza, Crisita Carmen Hojilla,Diao, Tianning,Weller, Keith J.,Nye, Susan A.,Lewis, Kenrick M.,Delis, Johannes G. P.,Boyer, Julie L.,Roy, Aroop K.,Chirik, Paul J.

supporting information, p. 12108 - 12118 (2014/10/16)

The aryl-substituted bis(imino)pyridine cobalt methyl complex, ( MesPDI)CoCH3 (MesPDI = 2,6-(2,4,6-Me 3C6H2-N=CMe)2C5H 3N), promotes the catalytic dehydrogenative silylation of linear α-olefins to selectively form the corresponding allylsilanes with commercially relevant tertiary silanes such as (Me3SiO) 2MeSiH and (EtO)3SiH. Dehydrogenative silylation of internal olefins such as cis- and trans-4-octene also exclusively produces the allylsilane with the silicon located at the terminus of the hydrocarbon chain, resulting in a highly selective base-metal-catalyzed method for the remote functionalization of C-H bonds with retention of unsaturation. The cobalt-catalyzed reactions also enable inexpensive α-olefins to serve as functional equivalents of the more valuable α, ω-dienes and offer a unique method for the cross-linking of silicone fluids with well-defined carbon spacers. Stoichiometric experiments and deuterium labeling studies support activation of the cobalt alkyl precursor to form a putative cobalt silyl, which undergoes 2,1-insertion of the alkene followed by selective β-hydrogen elimination from the carbon distal from the large tertiary silyl group and accounts for the observed selectivity for allylsilane formation.

Catalytic reactions of hydrosiloxanes with allyl chloride

Jankowiak, Marcin,MacIejewski, Hieronim,Gulinski, Jacek

, p. 4478 - 4487 (2007/10/03)

Catalytic reactivity of Si-H bond of di-, trisiloxanes with allyl chloride in the presence of platinum catalyst has been examined. Hydrosilylation process competes with hydrogen substitution by chlorine and/or propenyl group. The effect of the reaction conditions as well as structure of siloxane on the yield and selectivity of the number of products has been discussed. Several consecutive-competitive processes have been identified. The results obtained can be helpful in the study of the catalytic hydropolysiloxanes reactions with allyl derivatives-systems of great practical importance, to produce commercial functionalized silicones.

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