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1073338-97-2

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1073338-97-2 Usage

Uses

4-Bromo-3,5-dimethylphenylboronic Acid Pinacol Ester is useful as a reactant in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1073338-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1073338-97:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*3)+(3*8)+(2*9)+(1*7)=152
152 % 10 = 2
So 1073338-97-2 is a valid CAS Registry Number.

1073338-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1,3-dimethyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzene

1.2 Other means of identification

Product number -
Other names 4-bromo-3,5-dimethylphenyl boronic acid pinacol ester

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:1073338-97-2 SDS

1073338-97-2Relevant articles and documents

D-π-A triarylboron compounds with tunable push-pull character achieved by modification of both the donor and acceptor moieties

Zhang, Zuolun,Edkins, Robert M.,Nitsch, J?rn,Fucke, Katharina,Eichhorn, Antonius,Steffen, Andreas,Marder, Todd B.,Wang, Yue

, p. 177 - 190 (2015)

The push-pull character of a series of donor-bithienyl-acceptor compounds has been tuned by adopting triphenylamine or 1,1,7,7-tetramethyljulolidine as a donor and B(2,6-Me2-4-RC6H2)2 (R=Me, C6F5 or 3

NEW INDANYLOXYDIHYDROBENZOFURANYLACETIC ACIDS

-

Paragraph 0863, (2013/10/07)

The present invention relates to compounds of general formula I, wherein the groups R1, R2 and m are defined as in claim 1, which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

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