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1,3,4-Thiadiazol-2-amine, 5-(1,3-diphenyl-1H-pyrazol-4-yl)-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

521936-76-5

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521936-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 521936-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,1,9,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 521936-76:
(8*5)+(7*2)+(6*1)+(5*9)+(4*3)+(3*6)+(2*7)+(1*6)=155
155 % 10 = 5
So 521936-76-5 is a valid CAS Registry Number.

521936-76-5SDS

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 5-(1,3-diphenylpyrazol-4-yl)-N-phenyl-1,3,4-thiadiazol-2-amine

1.2 Other means of identification

Product number -
Other names 1,3,4-Thiadiazol-2-amine,5-(1,3-diphenyl-1H-pyrazol-4-yl)-N-phenyl

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:521936-76-5 SDS

521936-76-5Upstream product

521936-76-5Downstream Products

521936-76-5Relevant academic research and scientific papers

Synthesis and fluorescent properties of 2-arylamino-5-(3-aryl-1-phenyl- pyrazol-4-yl)-1,3,4-thiadiazoles

Li, Cun-Kui,Cao, Ling-Hua

experimental part, p. 1313 - 1316 (2009/12/04)

A series of novel pyrazolyl-substituted 1,3,4-thiadiazole derivatives (6a-6d, 7a-7d, 8a-8d) were prepared by cyclization of the intermediate 3-aryl-l-phenyl-pyrazol-4-ylformaldehyde 4′-phenylthiosemicarbazones with 0.5 M ferric chloride solution. The structures of the new compounds were confirmed by IR, 1H NMR and elemental analysis. Simultaneously, the compounds were detected by fluorescence spectrophotometer and had preferable fluorescence activity.

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