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Check Digit Verification of cas no

The CAS Registry Mumber 71530-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,3 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71530-61:
(7*7)+(6*1)+(5*5)+(4*3)+(3*0)+(2*6)+(1*1)=105
105 % 10 = 5
So 71530-61-5 is a valid CAS Registry Number.

71530-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-hydroxy-4-[(6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]benzoic acid

1.2 Other means of identification

Product number	-
Other names	Salicyliden-{4-amino-2-hydroxy-benzoesaeure}

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:71530-61-5 SDS

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71530-61-5Relevant academic research and scientific papers

The zwitterionic structure of 2-hy droxy-4-[(2-hy droxy benzyl idene)amino] benzoic acid

Junior, Anderson A. B. C.,De Carvalho, Gustavo S. G.,Marques, Lippy F.,Correa, Charlane C.,Da Silva, Adilson D.,Machado, Flavia C.

, p. 934 - 936 (2013)

The title compound, C14H11NO4, exists in the solid phase in the zwitterionic form, 2-{[(4-carb oxy-3-hy droxy phen yl)iminium yl]methyl}phenolate, with the H atom from the phenol group on the 2-hy droxy benzyl idene ring transferred to the imine N atom, r

Schiff base conjugates of p-aminosalicylic acid as antimycobacterial agents

Patole, Jayendra,Shingnapurkar, Dipti,Padhye, Subhash,Ratledge, Colin

, p. 1514 - 1517 (2007/10/03)

Schiff base conjugates of p-aminosalicylic acid have been synthesized and characterized by elemental analysis, IR and 1H NMR spectroscopy and cyclic voltammetry. Compounds containing hydroxyl-rich side chains show enhanced antimycobacterial act

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