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82859-78-7

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82859-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82859-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,5 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82859-78:
(7*8)+(6*2)+(5*8)+(4*5)+(3*9)+(2*7)+(1*8)=177
177 % 10 = 7
So 82859-78-7 is a valid CAS Registry Number.

82859-78-7SDS

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 Benzoic acid, m-nitro-, salicylidenehydrazide

1.2 Other means of identification

Product number -
Other names 3-nitroaniline-N-salicylidene

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:82859-78-7 SDS

82859-78-7Relevant articles and documents

Efficient synthesis of functionalized 1,3-dihydroisobenzofurans from salicylaldehydes: Application to the synthesis of escitalopram

Wang, Peng,Zhang, Rui,Cai, Jin,Chen, Jun-Qing,Ji, Min

, p. 549 - 552 (2014/05/06)

An efficient synthesis of substituted 1,3-dihydroisobenzofurans is developed. In this novel route, o-aroylbenzaldehydes, as key intermediates, can be obtained by lead tetraacetate oxidation of N-aroylhydrazones of salicylaldehydes. The mild and general st

A versatile and regiospecific synthesis of functionalized 1,3-diarylisobenzofurans

Jacq, Jerome,Einhorn, Cathy,Einhorn, Jacques

supporting information; experimental part, p. 3757 - 3760 (2009/07/01)

(Chemical Equation Presented) A convenient, versatile, and regiospecific synthesis of functionalized 1,3-diarylisobenzofurans has been developed. It involves chemoselective addition of arylmagnesium reagents to the aldehyde function of o-aroylbenzaldehydes, themselves readily obtained by lead tetraacetate oxidation of N-aroylhydrazones of salicylaldehydes. Various functional groups, including nitro, iodo, or ester functionalities, have thus been positioned with complete regiospecificity on the 1,3-diphenylisobenzofuran backbone.

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