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CAS

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93073-20-2

6-Phenyl-3-(phenylmethyl)-1,2,4-triazolo(3,4-b)(1,3,4)thiadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93073-20-2 Structure

  • Basic information

    1. Product Name: 6-Phenyl-3-(phenylmethyl)-1,2,4-triazolo(3,4-b)(1,3,4)thiadiazole
    2. Synonyms:
    3. CAS NO:93073-20-2
    4. Molecular Formula:
    5. Molecular Weight: 292.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93073-20-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-Phenyl-3-(phenylmethyl)-1,2,4-triazolo(3,4-b)(1,3,4)thiadiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Phenyl-3-(phenylmethyl)-1,2,4-triazolo(3,4-b)(1,3,4)thiadiazole(93073-20-2)
    11. EPA Substance Registry System: 6-Phenyl-3-(phenylmethyl)-1,2,4-triazolo(3,4-b)(1,3,4)thiadiazole(93073-20-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93073-20-2(Hazardous Substances Data)

93073-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93073-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,7 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93073-20:
(7*9)+(6*3)+(5*0)+(4*7)+(3*3)+(2*2)+(1*0)=122
122 % 10 = 2
So 93073-20-2 is a valid CAS Registry Number.

93073-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

1.2 Other means of identification

Product number -
Other names -

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:93073-20-2 SDS

93073-20-2Downstream Products

93073-20-2Relevant articles and documents

Microwave-enhanced reactions of 4-amino-5-merecapto-1,2,4-triazoles with benzoyl chloride and aromatic aldehydes

Bai, Yinjuan,Zhao, Guifang,Li, Chunyuan,Zhao, Shuixia,Shi, Zhen

, p. 3311 - 3319 (2008/12/22)

The microwave-enhanced reactions of 4-amino-5-mercapto-3-substituent-1,2,4- triazoles with benzoyl chloride or arylaldehydes under solvent-free conditions without catalyst were studied. 3-Substituded-6-phenyl-1,2,4-triazolo[3,4-b]-1,3, 4-thiadiazoles were

3,6-disubstituted 1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles: Synthesis, antimicrobial and antiviral activity. II

Invidiata,Simoni,Scintu,Pinna

, p. 659 - 664 (2007/10/03)

A series of novel 3,6-disubstituted 1,2,4-triazolo[3,4-b] [1,3,4]thiadiazole derivatives was prepared and tested to evaluate their antimycotic and antibacterial activities. Anti-HIV-1 activity has also been investigated. Among the test compounds, derivatives 10a-14a and 16c showed anti-HIV-1 activity at concentrations slightly below those cytotoxic. Substitutions at 3 and 6 positions seems to be important in lowering the cytotoxicity of compounds.

Synthesis and Pharmacology of 2-Aryl/aralkyl-5-aryl/aralkyl/diaralkyl-s-triazolo-1,3,4-thiadiazoles

Deshmukh, A. A.,Mody, M. K.,Ramalingam, T.,Sattur, P. B.

, p. 793 - 795 (2007/10/02)

A series of s-triazolo-1,3,4-thiadiazoles (III) carrying aryl or aralkyl group at 2-position and aryl, aralkyl or diaralkyl group at 5-position have been synthesised and evaluated for their biological activities.Some of the compounds exhibit strong CNS depressant and mild to moderate antiinflammatory action in experimental animals.

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