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68629-85-6

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68629-85-6 Usage

Appearance

Yellow solid

Molecular weight

232.28 g/mol

Chemical structure

A derivative of anthracene, a polycyclic aromatic hydrocarbon

Potential applications

a. Organic synthesis
b. Material science
c. Medicinal chemistry

Properties

a. Fluorescent, useful in research and development of optical materials
b. Potential biological activities

Utility

Can be used as a building block in the synthesis of other organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 68629-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68629-85:
(7*6)+(6*8)+(5*6)+(4*2)+(3*9)+(2*8)+(1*5)=176
176 % 10 = 6
So 68629-85-6 is a valid CAS Registry Number.

68629-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-sulfanylideneanthracen-9-one

1.2 Other means of identification

Product number -
Other names 1,3-Butadiene thioquinone

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:68629-85-6 SDS

68629-85-6Relevant articles and documents

Reaction of anthrone and its 1- and 4-substituted derivatives with sulfur in the presence of nucleophiles

Loskutov

, p. 1478 - 1481 (2007/10/03)

Anthrone and its 1-substituted derivatives react with molecular sulfur in the presence of nucleophiles (aromatic amines, hydrazine, substituted hydrazines, and malononitrile) to give intermediate monothioanthraquinones which are then converted into mixtures of the corresponding anthraquinones and 10-imino-, 10-hydrazono-, or 10-dicyanomethylene-9,10-dihydroanthracen-9-ones. Unlike 1-substituted derivatives, 4-substituted anthrones react with sulfur in the presence of phenylhydrazine to give only 1-substituted anthraquinones.

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