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

89145-08-4

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89145-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89145-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,4 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89145-08:
(7*8)+(6*9)+(5*1)+(4*4)+(3*5)+(2*0)+(1*8)=154
154 % 10 = 4
So 89145-08-4 is a valid CAS Registry Number.

89145-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 3-(4-chlorophenyl)-5-(2-thienyl)-pyrazoline

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:89145-08-4 SDS

89145-08-4Downstream Products

89145-08-4Relevant academic research and scientific papers

N1-benzenesulfonyl-2-pyrazoline hybrids in neurological disorders: Syntheses, biological screening and computational studies

Tripathi, Avinash C.,Upadhyay, Savita,Paliwal, Sarvesh,Saraf, Shailendra K.

, p. 126 - 148 (2018/02/14)

A novel series of 1,3,5-trisubstituted-2-pyrazolines (5a-5t) was prepared via Claisen Schmidt condensation, followed by heterocyclization with hydrazine hydrate, substitution of N1 hydrogen of 2-pyrazoline nucleus with 4-chlorobenzenesulfonylchloride, app

Derivatives of 4,5-dihydro (1H) pyrazoles as possible MAO-A inhibitors in depression and anxiety disorders: synthesis, biological evaluation and molecular modeling studies

Tripathi, Avinash C.,Upadhyay, Savita,Paliwal, Sarvesh,Saraf, Shailendra K.

, p. 1485 - 1503 (2018/03/29)

A series of 1,3,5-trisubstituted-2-pyrazoline derivatives (3a–3t) were synthesized in appreciable yields by substituting N1 position of 2-pyrazoline nucleus with 4-nitrobenzenesulfonylchloride using conventional and microwave assisted synthetic approaches

An expeditious one-pot microwave facilitated versus conventional syntheses: In vivo biological screening and molecular docking studies of some 3,5-disubstituted-4,5-dihydro-(1H)-pyrazole derivatives

Tripathi, Avinash C.,Upadhyay, Savita,Paliwal, Sarvesh,Saraf, Shailendra K.

, p. 390 - 406 (2016/02/19)

A series of 3,5-disubstituted-2-pyrazoline derivatives (2a-2t) were synthesized by reacting different aromatic/heteroaromatic aldehydes and ketones, in a two-step reaction through Claisen Schmidt condensation, followed by cyclization of the resulted chalc

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.

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