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108732-56-5

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108732-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108732-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,3 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108732-56:
(8*1)+(7*0)+(6*8)+(5*7)+(4*3)+(3*2)+(2*5)+(1*6)=125
125 % 10 = 5
So 108732-56-5 is a valid CAS Registry Number.

108732-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-o-nitrophenylthio-1,2-naphthoquinone

1.2 Other means of identification

Product number -
Other names .4-(2-Nitro-phenylmercapto)-[1,2]naphthochinon

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:108732-56-5 SDS

108732-56-5Relevant articles and documents

Quinones. Part 11. The Reaction of o-Aminothiophenol with o-Benzo- and o-Naphtho-quinones: A New Route to 1H-Phenothiazin-1-ones

Mackenzie, Neil E.,Surendrakumar, Sivagnanasundram,Thomson, Ronald H.,Cowe, Heather J.,Cox, Philip J.

, p. 2233 - 2242 (2007/10/02)

1H-Phenothiazin-1-ones can be obtained by the condensation of o-aminothiophenol with 3,5-di-t-butyl- and 3-t-butyl-5-phenyl-o-benzoquinones.In the absence of large blocking groups the phenothiazinones are unstable.A methyl group at C-4 leads via the quinone-methide tautomer, to formation of a spiro-dimer the crystal structure of which was determined by X-ray analysis.By further reaction with o-aminothiophenol, 1H-phenothiazin-1-ones yield triphenodithiazines (benzothiazinophenothiazines). o-Naphthoquinones do not form benzo-1H-phenothiazin-1-ones with o-aminothiophenol.The parent compound yields 4-hydroxy-3H-benzophenothiazin-3-one by initial thiol addition at C-4 followed by rearrangement.

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