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73642-91-8

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73642-91-8 Usage

Physical state

Colorless liquid at room temperature

Uses

a. Synthesis of pharmaceuticals
b. Synthesis of agrochemicals

Reactivity

Highly reactive due to the presence of two bromine atoms

Applications in chemical reactions

a. Cross-coupling reactions
b. Radical polymerization

Potential applications

a. Production of surfactants
b. Building block in the synthesis of novel organic compounds

Safety precautions

Toxic and can cause skin and eye irritation; handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 73642-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,4 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73642-91:
(7*7)+(6*3)+(5*6)+(4*4)+(3*2)+(2*9)+(1*1)=138
138 % 10 = 8
So 73642-91-8 is a valid CAS Registry Number.

73642-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dibromononane

1.2 Other means of identification

Product number -
Other names 1,2-Dibrom-nonan

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:73642-91-8 SDS

73642-91-8Relevant articles and documents

Facile one-pot synthesis of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent

Patil, Rajendra D.,Joshi, Girdhar,Adimurthy, Subbarayappa,Ranu, Brindaban C.

experimental part, p. 2529 - 2532 (2009/09/06)

A new method for the preparation of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent has been developed. Several α-bromoketones were successfully prepared from a variety of olefins by this method. This procedure is an alternative to conventional molecular bromine.

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