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106141-07-5

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106141-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106141-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106141-07:
(8*1)+(7*0)+(6*6)+(5*1)+(4*4)+(3*1)+(2*0)+(1*7)=75
75 % 10 = 5
So 106141-07-5 is a valid CAS Registry Number.

106141-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-pivaloyloxybenzene

1.2 Other means of identification

Product number -
Other names .2-bromophenyl pivalate

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:106141-07-5 SDS

106141-07-5Relevant articles and documents

Umpolung direct arylation reactions: Facile process requiring only catalytic palladium and substoichiometric amount of silver salts

Mousseau, James J.,Vallee, Frederic,Lorion, Melanie M.,Charette, Andre B.

, p. 14412 - 14414 (2010)

An umpolung direct arylation process is described. The reaction requires only a catalytic amount of Pd(OAc)2 and a substoichiometric amount of silver salts, without any external base or ligand to proceed. The directed oxidative insertion of the transition metal followed by the coupling into the C-H bond of an unactivated arene has surprisingly not yet been reported, despite the clear advantages in the ease of starting material synthesis. The reaction is regioselective with regards to the arene partner, and the role of the acetate and carbonate groups has been elucidated. This methodology adds to the very few examples of benzene coupling without the inclusion of electron-withdrawing groups to increase acidity.

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