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62127-60-0

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62127-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62127-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,2 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62127-60:
(7*6)+(6*2)+(5*1)+(4*2)+(3*7)+(2*6)+(1*0)=100
100 % 10 = 0
So 62127-60-0 is a valid CAS Registry Number.

62127-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dibromo-3-methylbutane

1.2 Other means of identification

Product number -
Other names 3,3-dibromo-2-methylpentane

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:62127-60-0 SDS

62127-60-0Downstream Products

62127-60-0Relevant articles and documents

Studies on the Synthesis of Heterocyclic Compounds. XIV. Cleavage of 1,3-Benzoxathioles by Magnesium Bromide-Acetic Anhydride

Bonsignore, Leonardo,Fadda, Anna Maria,Loy, Giuseppe,Maccioni, Anna Maria,Marongiu, Enrica,Podda, Gianni

, p. 573 - 576 (2007/10/02)

The cleavage reaction of some 1,3-benzoxathioles with magnesium bromide and acetic anhydride has been studied.In all the 1,3-benzoxathioles studied, the opening of the heterocyclic ring occurs first with cleavage of the C-O bond and formation of bromides and their corresponding products of hydrolysis.Successively also the cleavage of the C-S bond can occur.The competitive electrophilic substitution on the benzene ring becomes appreciable only in the 1,3-benzoxathioles-2,2-disubstituted with sterically demanding groups.The structure of newly prepared compounds has been determined by analytical and spectroscopic data and when possible by comparison with authentic samples.

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