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4-methyl-5-sulfanyl-benzene-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27320-24-7

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27320-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27320-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27320-24:
(7*2)+(6*7)+(5*3)+(4*2)+(3*0)+(2*2)+(1*4)=87
87 % 10 = 7
So 27320-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2S/c1-4-2-5(8)6(9)3-7(4)10/h2-3,8-10H,1H3

27320-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-5-sulfanylbenzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 2-Thio-4,5-dihydroxytoluene

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:27320-24-7 SDS

27320-24-7Upstream product

27320-24-7Downstream Products

27320-24-7Relevant academic research and scientific papers

A convenient access to dihydroxybenzenethiols via reduction of iso-thiouronium salts with sodium borohydride

Mascagna,D'Ischia,Costantini,Prota

, p. 35 - 42 (2007/10/02)

An improved procedure for the preparation of unstable dihydroxybenzenethiols in high yields is reported, involving mild reduction of the corresponding iso-thiouronium salts with sodium borohydride.

Synthesis, redox characteristics, and in vitro norepinephrine uptake inhibiting properties of 2-(2-mercapto-4,5-dihydroxyphenyl)ethylamine (6-mercaptodopamine)

Chavdarian,Castagnoli Jr.

, p. 1317 - 1322 (2007/10/06)

In an attempt to further characterize the structural features of 6-hydroxydopamine analogues that are associated with in vivo neuronal degeneration, the synthesis of 6-mercaptodopamine was undertaken. Although reaction conditions leading to the 1,4 additi

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