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2515-51-7

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2515-51-7 Usage

Structure

A five-membered aromatic ring with two nitrogen atoms at adjacent positions, with three phenyl groups attached to the 1, 3, and 4 positions.

Type

A derivative of pyrazole.

Usage

Commonly used in organic synthesis and pharmaceutical research as a building block for various biologically active molecules.

Potential applications

CNS stimulant, anticancer, and anti-inflammatory agent.

Corrosion inhibition

Has shown potential as a corrosion inhibitor for mild steel in acidic media.

Further research needed

To explore its full range of properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2515-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2515-51:
(6*2)+(5*5)+(4*1)+(3*5)+(2*5)+(1*1)=67
67 % 10 = 7
So 2515-51-7 is a valid CAS Registry Number.

2515-51-7SDS

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 1,3,4-triphenyl-4,5-dihydro-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 1,3,4-Triphenyl-pyrazolin

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:2515-51-7 SDS

2515-51-7Downstream Products

2515-51-7Relevant articles and documents

A novel methodology for synthesis of dihydropyrazole derivatives as potential anticancer agents

Wang, Xu,Pan, Ying-Ming,Huang, Xiao-Chao,Mao, Zhong-Yuan,Wang, Heng-Shan

supporting information, p. 2028 - 2032 (2014/03/21)

A novel, simple, and efficient method for the synthesis of 4,5-dihydropyrazole derivatives has been developed. The reaction proceeded through the base-induced isomerization of easily accessible propargyl alcohols followed by cyclization of α,β-unsaturated hydrazones. Furthermore, selected compounds 3ab and 3ac exhibited good activities against Bel-7404 (human hepatoma cancer), HepG2 (human liver cancer), NCI-H460 (human lung cancer) and SKOV3 (human ovarian cancer) cell lines with IC50 in the range of 22-46 μmol L-1.

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