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65983-49-5

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65983-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65983-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,8 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65983-49:
(7*6)+(6*5)+(5*9)+(4*8)+(3*3)+(2*4)+(1*9)=175
175 % 10 = 5
So 65983-49-5 is a valid CAS Registry Number.

65983-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-2-(2,3,4,5-tetrachlorophenyl)acetamide

1.2 Other means of identification

Product number -
Other names 3,4,5,6-Tetrachlorphenyl-glyoxalsaeureamid

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:65983-49-5 SDS

65983-49-5Downstream Products

65983-49-5Relevant articles and documents

Polyhalogenated Bicycloocta-1,5,7-trienes, XI. - Preparation and Reactions of Bicycloocta-1,3,5-trien-7,8-diyl Sulfates

Roedig, Alfred,Ganns, Eva Maria,Ganns, Rainer

, p. 1982 - 1994 (2007/10/02)

The cyclic sulfates 4a, d and e were prepared from 1a, d and e with sulfuric acid at room temperature.At a higher temperature the diketones 3a or b are produced.Thermolysis of the sulfates at 180-200 deg C as well as acidic hydrolysis lead likewise to 3a or b.Alkaline hydrolysis, however, yields the phthalides 5a or b.Analogous reaction courses are observed with alkoholates yielding 5c, d, f, methanethiolate giving 5e, and secondary amines 8a-f.Contrary, with ammonia and primary amines the phenylglyoxylic amides 13a-f are formed.The other ring opening products 9a, b, 10, and 11 are obtained from 4a with phenolates under different conditions.In the reactions 4 -> 8 the intermediates 6 and 7 can be isolated, so that some general mechanistic interpretations are possible.

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