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739336-26-6

739336-26-6

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739336-26-6 Usage

Chemical Properties

Off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 739336-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,9,3,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 739336-26:
(8*7)+(7*3)+(6*9)+(5*3)+(4*3)+(3*6)+(2*2)+(1*6)=186
186 % 10 = 6
So 739336-26-6 is a valid CAS Registry Number.

739336-26-6 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H62005)  2-Bromo-5-fluorophenyl acetic acid, 96%   

  • 739336-26-6

  • 1g

  • 1292.0CNY

  • Detail

  • Alfa Aesar

  • (H62005)  2-Bromo-5-fluorophenyl acetic acid, 96%   

  • 739336-26-6

  • 5g

  • 5061.0CNY

  • Detail

  • Alfa Aesar

  • (H62005)  2-Bromo-5-fluorophenyl acetic acid, 96%   

  • 739336-26-6

  • 25g

  • 21000.0CNY

  • Detail

739336-26-6SDS

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 2-Bromo-5-fluorophenylacetic acid

1.2 Other means of identification

Product number -
Other names 2-(2-bromo-5-fluorophenyl)acetic acid

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:739336-26-6 SDS

739336-26-6Downstream Products

739336-26-6Relevant articles and documents

Highly diastereoselective synthesis of tetralin-fused spirooxindoles via lewis acid-catalyzed C(sp3)H bond functionalization

Machida, Mizuki,Mori, Keiji

, p. 868 - 871 (2018/07/03)

A highly diastereoselective synthesis of tetralin-fused spirooxindole derivatives was described. Treatment of benzylidene oxindoles with a catalytic amount of Sc(OTf)3 in refluxing hexane afforded the target compounds in good chemical yields with excellent diastereoselectivities (up to >20:1). Detailed investigation of the reaction mechanism revealed that both interconversion of the two diastereomers and their solubility difference in reaction medium were the key to achieving excellent diastereoselectivities.

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