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17021-92-0

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17021-92-0 Usage

General Description

(4-bromophenyl)(methoxy)dimethylsilane is a chemical compound with the molecular formula C10H13BrOSi. It is a silane derivative containing a bromophenyl group, a methoxy group, and two dimethylsilane groups. (4-bromophenyl)(methoxy)dimethylsilane is primarily used in the synthesis of organic and organometallic compounds, as well as in the production of specialty chemicals. It may also be used as a reactant in the preparation of pharmaceuticals and agrochemicals. Additionally, it has potential applications in the development of materials and coatings due to its unique chemical and physical properties. Overall, (4-bromophenyl)(methoxy)dimethylsilane plays a crucial role in various chemical and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 17021-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,2 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17021-92:
(7*1)+(6*7)+(5*0)+(4*2)+(3*1)+(2*9)+(1*2)=80
80 % 10 = 0
So 17021-92-0 is a valid CAS Registry Number.

17021-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromophenyl)-methoxy-dimethylsilane

1.2 Other means of identification

Product number -
Other names p-Bromphenyldimethylmethoxysilan

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:17021-92-0 SDS

17021-92-0Downstream Products

17021-92-0Relevant articles and documents

Synthesis of phenols via fluoride-free oxidation of arylsilanes and arylmethoxysilanes

Rayment, Elizabeth J.,Summerhill, Nick,Anderson, Edward A.

, p. 7052 - 7060 (2012/10/07)

Rapid, efficient methods have been developed to prepare phenols from the oxidation of arylhydrosilanes. The effects of arene substituents and fluoride promoters on this process show that while electron-deficient arenes can undergo direct oxidation from the hydrosilane, electron-rich aromatics benefit from silane activation via oxidation to the methoxysilane using homogeneous or heterogeneous transition metal catalysis. The combination of these two oxidations into a streamlined flow procedure involving minimal processing of reaction intermediates is also reported.

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