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24373-98-6

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24373-98-6 Usage

Classification

Brominated indene (organic compounds containing bromine and an indene ring structure)

Usage

Building block for more complex molecules in organic synthesis and chemical research

Industry applications

Pharmaceutical and agrochemical industries

Chemical properties

Valuable tool in the development of new drugs, pesticides, and other useful compounds

Handling precautions

Potential health and environmental hazards if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 24373-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,7 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24373-98:
(7*2)+(6*4)+(5*3)+(4*7)+(3*3)+(2*9)+(1*8)=116
116 % 10 = 6
So 24373-98-6 is a valid CAS Registry Number.

24373-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 1-indanyl bromide

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:24373-98-6 SDS

24373-98-6Relevant articles and documents

Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides

Arp, Forrest O.,Fu, Gregory C.

, p. 10482 - 10483 (2007/10/03)

This report describes the first enantioselective cross-couplings of racemic secondary benzylic halides, specifically, nickel-catalyzed Negishi reactions of bromides and chlorides. The catalyst components are commercially available and air-stable, and the reaction is not highly oxygen- or moisture-sensitive (it can be set up in the air). The method has been applied to the catalytic enantioselective synthesis of intermediates employed by others in the generation of bioactive compounds (e.g., trikentrin A and an androgen receptor agonist). Copyright

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