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Hexadecane, 1,2-dibromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63758-87-2

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63758-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63758-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,5 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63758-87:
(7*6)+(6*3)+(5*7)+(4*5)+(3*8)+(2*8)+(1*7)=162
162 % 10 = 2
So 63758-87-2 is a valid CAS Registry Number.

63758-87-2SDS

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 1,2-dibromohexadecane

1.2 Other means of identification

Product number -
Other names Hexadecane, 1,2-dibromo-

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:63758-87-2 SDS

63758-87-2Relevant academic research and scientific papers

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.

OXIDATION OF N-ALKYL-N'-TOSYLHYDRAZINES WITH BROMINE

Palmieri, Gianni

, p. 4097 - 4102 (2007/10/02)

Oxidation of N-alkyl-N'-tosylhydrazines with bromine yield alkyl bromides, vicinal alkyl dibromides and traces of alcohols.The main products of primary hydrazines are monobromides whereas secondary hydrazines preferably produce dibromides.The reaction proceeds with evolution of nitrogen and hydrobromic acid and by the formation of intermediate sulfinic ester wich may be isolated.Various substrates were examined under different conditions to confirm the validity of the reaction mechanism hypothesized.

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