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140406-03-7

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140406-03-7 Usage

Molecular structure

Contains a benzodioxol ring, a triazole ring, and a phenylethanone group.

Chemical bonding

The benzodioxol and triazole rings are connected through a sulfur atom bonded to the triazole ring.

Potential applications

May have applications in the field of medicinal chemistry due to pharmacological activities of benzodioxol and triazole derivatives.

Need for further research

Additional studies are required to determine the specific properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 140406-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,0 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140406-03:
(8*1)+(7*4)+(6*0)+(5*4)+(4*0)+(3*6)+(2*0)+(1*3)=77
77 % 10 = 7
So 140406-03-7 is a valid CAS Registry Number.

140406-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanyl]-1-phenylethanone

1.2 Other means of identification

Product number -
Other names Ethanone,2-((5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl)thio)-1-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:140406-03-7 SDS

140406-03-7Relevant articles and documents

Synthesis and biological evaluation of thiazolo-triazole derivatives

Pignatello,Mazzone,Panico,Mazzone,Pennisi,Castana,Matera,Blandino

, p. 929 - 938 (2007/10/02)

Two series of isomeric thiazolo[3,2-b][1,2,4]triazole and thiazolo[2,3-c][1,2,4]triazole derivatives were prepared following multiple synthetic pathways. The obtained compounds were submitted to preliminar pharmacological assays to evaluate their anti-inf

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