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902120-00-7

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902120-00-7 Usage

General Description

Tert-Butyldimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)silane is a chemical compound that belongs to the class of organosilicon compounds. It is composed of a tert-butyldimethylsilyl group attached to a phenoxy group, which in turn is linked to a dioxaborolane ring. tert-Butyldimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)silane is often used as a reagent in organic synthesis, particularly in the formation of carbon-silicon bonds. Its unique structure and reactivity make it a valuable tool in the development of new drugs, materials, and other important chemical compounds. Additionally, its silicon and boron containing groups give it potential applications in the field of semiconductor technology and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 902120-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,1,2 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 902120-00:
(8*9)+(7*0)+(6*2)+(5*1)+(4*2)+(3*0)+(2*0)+(1*0)=97
97 % 10 = 7
So 902120-00-7 is a valid CAS Registry Number.

902120-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-dimethyl-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]silane

1.2 Other means of identification

Product number -
Other names 4,4,5,5-tetramethyl-2-(3-tert-butyldimethylsilyloxyphenyl)-1,3-dioxaborolane

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:902120-00-7 SDS

902120-00-7Relevant articles and documents

Synthesis of (S)-(-)-N-acetylcolchinol using intramolecular biaryl oxidative coupling

Besong, Gilbert,Jarowicki, Krzysztof,Kocienski, Philip J.,Sliwinski, Eric,Boyle, F. Thomas

, p. 2193 - 2207 (2008/02/09)

An asymmetric synthesis of the tubulin polymerisation inhibitor (S)-(-)-N-acetylcolchinol is reported based on an intramolecular biaryl oxidative coupling of a 1,3-diarylpropyl acetamide intermediate using phenyliodonium bis(trifluoroacetate) as the final

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