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(2E)-1-phenyl-3-[2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl]prop-2-en-1-one is a complex organic compound belonging to the thiadiazole family. It features a thiadiazole ring fused with a propenone group and a phenylamino substituent, which may contribute to its biological activity. (2E)-1-phenyl-3-[2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl]prop-2-en-1-one is of interest to researchers in medicinal chemistry and drug discovery due to its unique molecular structure and potential therapeutic applications.

125791-41-5

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125791-41-5 Usage

Uses

Used in Medicinal Chemistry:
(2E)-1-phenyl-3-[2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl]prop-2-en-1-one is used as a potential drug candidate for various diseases due to its unique molecular structure and the presence of a phenylamino group, which may contribute to its biological activity.
Used in Drug Discovery:
(2E)-1-phenyl-3-[2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl]prop-2-en-1-one is used in drug discovery research to explore its potential as a therapeutic agent. Its complex molecular structure and the presence of a phenylamino group make it a promising candidate for further study and development.
Used in Materials Science:
(2E)-1-phenyl-3-[2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl]prop-2-en-1-one may also have applications in materials science, although further research is needed to elucidate its full range of properties and potential uses in this field.
Used in Organic Synthesis:
(2E)-1-phenyl-3-[2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl]prop-2-en-1-one can be used as a building block or intermediate in organic synthesis for the development of new organic compounds and materials. Its unique structure and functional groups make it a valuable component in the synthesis of various organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 125791-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,9 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125791-41:
(8*1)+(7*2)+(6*5)+(5*7)+(4*9)+(3*1)+(2*4)+(1*1)=135
135 % 10 = 5
So 125791-41-5 is a valid CAS Registry Number.

125791-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(5-anilino-2-phenyl-2H-1,3,4-thiadiazol-3-yl)-1-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-Phenyl-3-(2-phenyl-5-(phenylamino)-1,3,4-thiadiazol-3(2H)-yl)-2-propen-1-one

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:125791-41-5 SDS

125791-41-5Downstream Products

125791-41-5Relevant academic research and scientific papers

THE REACTION OF TERMINAL α-ACETYLENIC KETONES WITH THIOSEMICARBAZONES

Komarova, T. N.,Nakhmanovich, A. S.,Sigalov, M. V.,Glotova, T. E.

, p. 1058 - 1060 (2007/10/02)

The reaction of terminal α-acetylenic ketones with thiosemicarbazones gives a series of 5-amino- and 5-anilino-3-acylvinyl-Δ4-1,3,4-thiadiazolines.These products react with perchloric acid to give the corresponding perchlorates.

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