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1033132-04-5

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1033132-04-5 Usage

General Description

1-benzyl-3-(trifluoromethyl)-1H-pyrazole is a chemical compound with the molecular formula C13H11F3N2. It is a pyrazole derivative that contains a benzyl group and a trifluoromethyl group. 1-benzyl-3-(trifluoromethyl)-1H-pyrazole has been studied for its potential use in pharmaceuticals, as it exhibits various biological activities. It has been found to have anti-inflammatory, analgesic, and anti-cancer properties, and has been investigated for its potential as a drug candidate. Additionally, 1-benzyl-3-(trifluoromethyl)-1H-pyrazole has shown to act as an insecticide, with potential applications in pest control. Its diverse range of properties makes it an interesting compound for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1033132-04-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,1,3 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1033132-04:
(9*1)+(8*0)+(7*3)+(6*3)+(5*1)+(4*3)+(3*2)+(2*0)+(1*4)=75
75 % 10 = 5
So 1033132-04-5 is a valid CAS Registry Number.

1033132-04-5Relevant articles and documents

Regioselective Synthesis, NMR, and Crystallographic Analysis of N1-Substituted Pyrazoles

Huang, Adrian,Wo, Kellie,Lee, So Yeun Christine,Kneitschel, Nika,Chang, Jennifer,Zhu, Kathleen,Mello, Tatsiana,Bancroft, Laura,Norman, Natalie J.,Zheng, Shao-Liang

, p. 8864 - 8872 (2017/09/11)

A systematic study of the N-substitution reactions of 3-substituted pyrazoles under basic conditions has been undertaken. Regioselective N1-alkylation, -arylation, and -heteroarylation of 3-substituted pyrazoles have been achieved using K2CO3-DMSO. The regioselectivity is justified by the DFT calculations at the B3LYP/6-31G??(d) level. A consistent steric effect on chemical shift has been observed for N-alkyl pyrazole analogues. Twenty-five X-ray crystallographic structures have been obtained to confirm the regiochemistry of the major products.

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