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1H-Pyrazole, 4,5-dihydro-1,3-diphenyl-5-(2-thienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2755-72-8

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2755-72-8 Usage

Chemical structure

1H-Pyrazole, 4,5-dihydro-1,3-diphenyl-5-(2-thienyl)-

Synonyms

Cetiedil

Type of compound

Synthetic organic compound, pyrazole derivative

Pharmacological properties

Anti-inflammatory, analgesic, potential antitumor and antileishmanial activities

Molecular weight

334.44 g/mol

Appearance

Not provided in the material

Solubility

Not provided in the material

Melting point

Not provided in the material

Boiling point

Not provided in the material

Research status

Investigated in animal studies for its ability to reduce pain and inflammation, potential candidate for the development of new drugs for treating these conditions, further research needed to fully understand its mechanisms of action and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2755-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2755-72:
(6*2)+(5*7)+(4*5)+(3*5)+(2*7)+(1*2)=98
98 % 10 = 8
So 2755-72-8 is a valid CAS Registry Number.

2755-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenyl-5-(thiophen-2-yl)-4,5-dihydro-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 1,3-diphenyl-5-thiophen-2-yl-4,5-dihydro-1H-pyrazole

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:2755-72-8 SDS

2755-72-8Relevant academic research and scientific papers

Synthesis and structural studies of isomeric Δ2- pyrazolines

Ingle,Doshi,Raut

experimental part, p. 1517 - 1520 (2011/10/13)

1-(2′-Thienyl)-3-(4″-dimethylamino phenyl)-2-propen-1-one(la-e) react with hydrazine hydrochloride in DMF medium to give isomeric 1-H pyrazolines (lla-e), react with phenyl hydrazine hydrochloride in DMF medium to give isomeric 1 -phenyl pyrazolines (Illa

Synthesis of and pharmacological studies on the antidepressant and anticonvulsant activities of some 1,3,5-trisubstituted pyrazolines

Ruhoglu, Ozan,Oezdemir, Zuhal,Calis, Uensal,Guemuesel, Buelent,Bilgin, Abdullah Altan

, p. 431 - 436 (2007/10/03)

Eighteen 1-phenyl-, 1-thiocarbamoyl- and 1-N-substitutedthiocarbamoyl-3- phenyl-5-heteroaryl-2-pyrazoline derivatives were synthesized and tested for their antidepressant and anticonvulsant activities. Their chemical structures were proved by spectral and microanalysis. The antidepressant activities of the compounds were investigated by the "forced swimming test". Results showed that compounds II-a,b,c, III-1b,1c,4a showed activities equivalent to or higher than pargyline hydrochloride (CAS 306-07-0) and tranylcypromine sulfate (CAS 13492-01-8) that were used as reference antidepressant drugs. Anticonvulsant activities of the compounds were determined by maximal electroshock seizure (MES), subcutaneous metrazol (ScMet.) and rotarod toxicity tests in mice according to the phase I tests of the Antiepileptic Drug Development programme. Compounds I-a, II-a,b,c, III-1b,2a,2c were found protective against MES and III-1b,1c,2a,2c were found protective against ScMet. ECV · Editio Cantor Verlag.

Heterocycles. 3. Synthesis and Spectral Data of Some 2-Pyrazolines

El-Rayyes, Nizar R.,Hovakeemian, George H.,Hmoud, Hayat S.

, p. 225 - 229 (2007/10/02)

The reaction of 1,3-diaryl-2-propen-1-ones (Ia-o) with hydrazine and methyl- and phenylhydrazine produced different substituted 2-pyrazolines (III).The structures of these products were evident from their chemical and spectroscopic analysis.

Thienyl acrylamides and thienyl pyrazolines as potential schistosomicidal agents

El Kerdawy,Samour,El Agamey

, p. 76 - 77 (2007/10/08)

α Thienyl N substituted acrylamides that possess analogous structures to known schistosomicidal agents were synthesized. Two chalcones were prepared by condensing α thiophenealdehyde and acetophenone or its o hydroxy derivative. Cyclization of the chalcon

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