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3-phenyl-1-(phenylcarbonyl)-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-5-ol is a complex organic compound with a molecular formula of C17H13F3N2O2. It features a pyrazol-5-ol core structure, which is a heterocyclic ring system containing nitrogen and oxygen atoms. The compound is characterized by a phenyl group (C6H5) attached to the 3-position of the pyrazol ring, a phenylcarbonyl (benzoyl) group at the 1-position, and a trifluoromethyl (CF3) group at the 5-position. The 4,5-dihydro prefix indicates that the compound has two hydrogen atoms attached to the 4 and 5 positions of the pyrazol ring, making it a dihydro derivative. This molecule is likely to be of interest in medicinal chemistry and materials science due to its unique structure and potential for various applications, such as in the development of pharmaceuticals or as a building block for more complex molecules.

5660-33-3

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5660-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5660-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5660-33:
(6*5)+(5*6)+(4*6)+(3*0)+(2*3)+(1*3)=93
93 % 10 = 3
So 5660-33-3 is a valid CAS Registry Number.

5660-33-3SDS

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 [5-hydroxy-3-phenyl-5-(trifluoromethyl)-4H-pyrazol-1-yl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names HMS2879K05

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:5660-33-3 SDS

5660-33-3Downstream Products

5660-33-3Relevant academic research and scientific papers

Copper(I)-catalyzed benzylic C(sp3)–H geminal difunctionalization: Successive oxidative intramolecular amidation and hydroxylation

Zhang, Zhiguo,Wang, Songnan,Hu, Chunfang,Ma, Nana,Zhang, Guisheng,Liu, Qingfeng

, p. 7472 - 7479 (2018/11/27)

A selective copper(I)-catalyzed benzylic C(sp3)–H geminal difunctionalization reaction of a benzylic-type sp3 carbon was developed. This novel strategy allowed simultaneous introduction of amide and hydroxyl group in a highly selecti

Synthesis and spectral properties of unsymmetrical benzoporphyrins containing phenoxy groups or quinoxaline fragments

Galanin,Shaposhnikov

, p. 1080 - 1086 (2008/09/16)

Condensation of phthalimide and 4-tert-butylphthalimide with zinc(II) acetate gave 3-(3-oxo-2,3-dihydro-1H-isoindol-1-ylidenemethyl)-1H-isoindol-1-one and 5-tert-butyl-3-(5-tert-butyl-3-oxo-2,3-dihydro-1H-isoindol-1-ylidenemethyl) -1H-isoindol-1-one, resp

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