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1,2,4-Thiadiazole-5(2H)-thione, 3-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20069-37-8

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20069-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20069-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20069-37:
(7*2)+(6*0)+(5*0)+(4*6)+(3*9)+(2*3)+(1*7)=78
78 % 10 = 8
So 20069-37-8 is a valid CAS Registry Number.

20069-37-8SDS

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-(4-methylphenyl)-2H-1,2,4-thiadiazole-5-thione

1.2 Other means of identification

Product number -
Other names F2184-0184

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:20069-37-8 SDS

20069-37-8Relevant academic research and scientific papers

Synthesis of 3,5-disubstituted-5,6-dihydro-4h-1,2,5-oxadiazine-6-thiones 1 and 3,5-disubstituted-1,2,4-thiadiazoles

Agirbas, Hikmet,Dueruest, Yasar,Karahasanoglu, Aysun

, p. 173 - 178 (2007/10/03)

3,5-Disubstituted-5,6-dihydro-4H-1,2,5-oxadiazine-6-thiones are prepared by the reaction of acetophenone oximes with thiophosgene. The thermal rearrangement of 3-phenyl-5-(p-tolyl)-5,6-dihydro-4H-1,2,5-oxadiazine-6-thione yields the corresponding 1,2,5-th

SYNTHESIS AND METHYLATION OF SOME 1,2,4-THIADIAZOLE--5-THIONES

Agirbas, Hikmet,Durust, Yasar,Sumengen, Dogan

, p. 321 - 324 (2007/10/02)

3,4-Disubstituted-1,2,4-thiadiazole-5(4H)-thiones (4) have been prepared by the treatment of 3,4-disubstituted-1,2,4-thiadiazole-5(4H)-ones (3) with P4S10.S-Methyl derivatives were obtained from the methylation of 3-substituted-1,2,4-thiadiazole-5(4H)-thi

1,3-Dipolar Cycloaddition Reactions of Nitrilium Betaines with Aryl Thiocyanates and Selenocyanates

Greig, Derek J.,Hamilton, Douglas G.,McPherson, Michael,Paton, R. Michael,Crosby, John

, p. 607 - 612 (2007/10/02)

The carbon-nitrogen triple bond of aryl thiocyanates acts as a dipolarophile in 1,3-dipolar cycloadditions.Reaction with nitrile oxides, nitrile sulphides, and benzonitrile N-phenylimide yields, respectively, 5-arylthio-1,2,4-oxadiazoles, -thidiazoles and -triazoles.Aryl selenocyanates behave similarly forming 5-arylseleno-1,2,4-oxadiazoles and -thiadiazoles from nitrile oxides and sulphides.Divergent pathways are followed by the reactions of secondary amines such as piperidine with 5-arylthio-1,2,4-oxadiazoles and -thidiazoles, the former yielding 5-piperidyl-1,2,4-oxadiazoles and the latter dihydro-1,2,4-thiadiazole-5-thiones.

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