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103028-42-8

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103028-42-8 Usage

Structure

Brominated derivative of 1H-indene

Usage

Building block in organic synthesis

Applications

Production of pharmaceuticals, agrochemicals, and other fine chemicals

Chemical reactivity

Unique

Bromine substituent

Makes it a versatile starting material for the synthesis of various organic compounds

Industrial use

Production of specialty polymers and other applications

Diverse range

Of chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 103028-42-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,2 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103028-42:
(8*1)+(7*0)+(6*3)+(5*0)+(4*2)+(3*8)+(2*4)+(1*2)=68
68 % 10 = 8
So 103028-42-8 is a valid CAS Registry Number.

103028-42-8SDS

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 3-bromo-1H-indene

1.2 Other means of identification

Product number -
Other names 3-bromo-indene

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:103028-42-8 SDS

103028-42-8Relevant articles and documents

Competitive, substrate-dependent reductive debromination/dehydrobromination of 1,2-dibromides with triethylamine

McGraw, Kristen M.,Kent, Greggory T.,Gonzalez, Joseph R.,Erden, Ihsan,Wu, Weiming

, p. 1973 - 1975 (2017/04/27)

The interaction of various 1,2-dibromides with NEt3 under various conditions (THF and DMF, respectively) at different temperatures was investigated. Our results from these reactions show that substrate dependent dehydrobrominations compete with reductive debrominations. A comprehensive discussion of these competitive pathways is offered.

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