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Trimethyl(pent-1-en-3-yloxy)silane is an organosilicon compound with the chemical formula C8H18OSi. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 158.31 g/mol. trimethyl(pent-1-en-3-yloxy)silane is characterized by a silicon atom bonded to three methyl groups and a pent-1-en-3-yloxy group, which consists of a pentene chain with an oxygen atom attached to the third carbon. Trimethyl(pent-1-en-3-yloxy)silane is primarily used as a coupling agent in the synthesis of various materials, such as ceramics, resins, and composites, to improve their mechanical properties and adhesion. It is also employed as a reagent in organic synthesis and as a silylating agent in the protection of alcohols and other functional groups. Due to its reactivity and potential hazards, it is essential to handle trimethyl(pent-1-en-3-yloxy)silane with care and in accordance with proper safety protocols.

18388-22-2

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18388-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18388-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,8 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18388-22:
(7*1)+(6*8)+(5*3)+(4*8)+(3*8)+(2*2)+(1*2)=132
132 % 10 = 2
So 18388-22-2 is a valid CAS Registry Number.

18388-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(pent-1-en-3-yloxy)silane

1.2 Other means of identification

Product number -
Other names trimethyl-pent-1-en-3-yloxy-silane

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:18388-22-2 SDS

18388-22-2Relevant academic research and scientific papers

Isomerization of allylic silyl ethers catalyzed by ReO3(OSiR3) complexes

Bellemin-Laponnaz, Stéphane,Le Ny, Jean Pierre,Osborn, John A.

, p. 1549 - 1552 (2007/10/03)

Efficient isomerization of allylic alcohols and allylic ethers at room temperature by rhenium (VII) oxo complexes is described. (C) 2000 Elsevier Science Ltd.

General approach to halogenated tetrahydrofuran natural products from red algae of the genus Laurencia. Total synthesis of (±)-trans-kumausyne and demonstration of an asymmetric synthesis strategy

Brown, Mark J.,Harrison, Timothy,Overman, Larry E.

, p. 5378 - 5384 (2007/10/02)

A general strategy for the synthesis of C15 halogenated tetrahydrofuranoid lipids from red algae of the genus Laurencia has been developed. The central step is the convenient formation of hydrobenzofuranone (±)-5 on a large scale, and with comp

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