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103931-15-3

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103931-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103931-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,3 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103931-15:
(8*1)+(7*0)+(6*3)+(5*9)+(4*3)+(3*1)+(2*1)+(1*5)=93
93 % 10 = 3
So 103931-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2S/c1-10-6-4-2-3-5(8)7(6)9/h2-4,8-9H,1H3

103931-15-3SDS

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 3-methylsulfanylbenzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 3-MTC

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:103931-15-3 SDS

103931-15-3Downstream Products

103931-15-3Related news

Reactions of 3-ethylcatechol and 3-(methylthio)catechol with catechol dioxygenases07/20/2019

The reactions of 3-ethylcatechol and 3-(methylthio)catechol with catechol 1,2-dioxygenase and catechol 2,3-dioxygenase from Pseudomonas putida were examined. Both 3-substituted catechols are oxidized by catechol 2,3-dioxygenase at approximately 30% of the rate observed for catechol oxidation by ...detailed

103931-15-3Relevant articles and documents

Iodine-Mediated Synthesis of Methylthio-Substituted Catechols from Cyclohexanones

Wu, Yue-Hua,Wang, Nai-Xing,Zhang, Tong,Yan, Zhan,Xu, Bao-Cai,Inoa, Joan,Xing, Yalan

, p. 3008 - 3013 (2019)

A novel and efficient I2-mediated direct synthesis of methylthio-substituted catechols from cyclohexanones was developed. Various cyclohexanones underwent oxygenation, methylthiolation, and dehydrogenative aromatization in one pot to form the desired products in moderate to good yields. DMSO was utilized as the solvent, oxygen source, and methylthiolation agent. A possible reaction mechanism is proposed. (Figure presented.).

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