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1H-Isoindole-1,3(2H)-dione, 2-[(5-[1,1'-biphenyl]-2-yl-1,3,4-thiadiazol-2-yl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104090-72-4

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104090-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104090-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,9 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104090-72:
(8*1)+(7*0)+(6*4)+(5*0)+(4*9)+(3*0)+(2*7)+(1*2)=84
84 % 10 = 4
So 104090-72-4 is a valid CAS Registry Number.

104090-72-4SDS

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 2-(2-biphenylyl)-5-(phthalimidomethyl)-1,3,4-thiadiazole

1.2 Other means of identification

Product number -
Other names 2-(5-Biphenyl-2-yl-[1,3,4]thiadiazol-2-ylmethyl)-isoindole-1,3-dione

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:104090-72-4 SDS

104090-72-4Downstream Products

104090-72-4Relevant academic research and scientific papers

Substituted 1,3,4-Thiadiazoles with Anticonvulsant Activity. 2. Aminoalkyl Derivatives

Stillings, Michael R.,Welbourn, Anthony P.,Walter, Donald S.

, p. 2280 - 2284 (2007/10/02)

This paper describes the synthesis and pharmacological evaluation of a number of substituted 1,3,4-thiadiazoles.The first member of the series, 2-(aminomethyl)-5-(2-biphenylyl)-1,3,4-thiadiazole (7) was found to possess potent anticonvulsant properties in rats and mice and compared favorably with the standard anticonvulsant drugs phenytoin, phenobarbital, and carbamazepine in a number of test situations.The potency of compound 7 was maintained on alkylation of the side-chain nitrogen atom; however, aryl substitution or chain lengthening caused a drop in potency.Replacement of the 2-biphenylyl group by phenyl or benzyl also lead to inactive compounds.

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