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7111-93-5

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7111-93-5 Usage

Class

Hetrocyclic compound

Subclass

Oxadiazoles

Functional group

Thione

Substituents

Methyl and phenyl

Potential applications

a. Pharmaceutical industry
b. Antimicrobial and antifungal properties
c. Corrosion inhibitor in metal coatings
d. Materials science
e. Organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 7111-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7111-93:
(6*7)+(5*1)+(4*1)+(3*1)+(2*9)+(1*3)=75
75 % 10 = 5
So 7111-93-5 is a valid CAS Registry Number.

7111-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-5-phenyl-1,3,4-oxadiazole-2-thione

1.2 Other means of identification

Product number -
Other names 3-methyl-5-phenyl-3H-[1,3,4]oxadiazole-2-thione

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:7111-93-5 SDS

7111-93-5Relevant articles and documents

Platinum assisted cyclization of S-methyl 3-acyl-2-methyldithiocarbazates under mild conditions. Crystal structure of [Pt2(μ-SMe)-(terpy)2][ClO4]3

Annibale, Giuliano,Bergamini, Paola,Bertolasi, Valerio,Cattabriga, Michela,Lazzaro, Antonio,Marchi, Andrea,Vertuani, Gianni

, p. 3877 - 3882 (1999)

The reaction of the newly synthesized aqua complex [Pt(terpy)(OH2)][BF4]2 with S-methyl 3-acyl-2-methyldithiocarbazates under a variety of experimental conditions has been studied. Using a 2:1 metal to ligand ratio in meth

Alkyl 2-Methyldithiocarbazates in Heterocyclic Synthesis: Preparation of 2-Alkylthio-1,3,4-thiadiazolium Cations and 2-Thioxo-2,3-dihydro-1,3,4-oxadiazole Derivatives

Molina, P.,Tarraga, A.,Espinosa, A.

, p. 690 - 693 (2007/10/02)

Alkyl 3-acyl-2-methyldithiocarbazates 2, available from alkyl 2-methyldithiocarbazates and acyl chlorides, undergo ring closure by the action of perchloric acid/acetic anhydride to give 2-alkylthio 3-methyl-1,3,4-thiadiazolium salts 4.Compounds 2 also und

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