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82969-01-5

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82969-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82969-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82969-01:
(7*8)+(6*2)+(5*9)+(4*6)+(3*9)+(2*0)+(1*1)=165
165 % 10 = 5
So 82969-01-5 is a valid CAS Registry Number.

82969-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,benzene-1,4-diol,4-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 1,4-Benzenediol,acetate 4-methylbenzenesulfonate

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:82969-01-5 SDS

82969-01-5Relevant articles and documents

Unusual Reaction of Azoxybenzenes with p-Toluenesulfonic Acid in Acetic Anhydride

Shimao, Ichiro,Fujimori, Ken,Oae, Shigeru

, p. 1538 - 1542 (2007/10/02)

Treatment of azoxybenzene with p-toluenesulfonic acid in acetic anhydride gave tosylates of 4- and 2-(phenylazo)phenols, and the corresponding acetates as by-product, besides azobenzene.However, a similar reaction of 4,4'-difluoroazoxybenzene gave 2-tosyloxy-4,4'-difluoroazobenzene as rearrangement product, besides 4-fluorophenyl tosylate and 4-fluorophenyl acetate.Meanwhile, the reaction of 4,4'-diacetoxyazoxybenzene afforded 4-acetoxyphenyl tosylate and hydroquinone diacetate in high yields.These unique reactions involve C-N bond cleavage, and may proceed through a pathway involving formation of benzenediazonium ion as the key intermediate.

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