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87338-03-2

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87338-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87338-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87338-03:
(7*8)+(6*7)+(5*3)+(4*3)+(3*8)+(2*0)+(1*3)=152
152 % 10 = 2
So 87338-03-2 is a valid CAS Registry Number.

87338-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-1,1-dimethoxy-1-phenylpropane

1.2 Other means of identification

Product number -
Other names -

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:87338-03-2 SDS

87338-03-2Relevant articles and documents

A Lewis Acid Catalyzed 1,2 Aryl Shift in α-Haloalkyl Aryl Acetals: A Convenient Route to α-Arylalkanoic Acids

Castaldi, Graziano,Belli, Aldo,Uggeri, Fulvio,Giordano, Claudio

, p. 4658 - 4661 (1983)

A new method for the synthesis of α-arylalkanoic acids is given, based on Lewis acid promoted rearrangement of acetals of primary and secondary α-haloalkyl aryl ketones (halo = Br, Cl) in hydrocarbon solvents.The reaction is selective, providing the esters of α-arylalkanoic acids in almost quantitative yields.The ability of "soft and borderline" Lewis acids in activating the carbon-halogen bond is compared with that of silver salts.The reaction mechanism is discussed.The present synthesis has been applied to some α-arylpropionic acids well-known as antiinflammatory drugs.

ELAECTROCHEMICAL OXIDATION OF CONJUGATED ARYLOLEFINS TO α-BROMOKETALS

Nikishin, Gennady I.,Elinson, Michail N.,Makhova, Irina V.

, p. 1603 - 1604 (2007/10/02)

Conjugated arylolefins electrolyzed in alcohols in the presence of alkali metal bromides are transformed into α-bromoketals.

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