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4-Hydroxy-1-phenylpyrazole is a chemical compound with the molecular formula C9H8N2O. It is a derivative of pyrazole, a heterocyclic organic compound consisting of a five-membered ring with two nitrogen atoms and three carbon atoms. The 4-hydroxy group indicates the presence of a hydroxyl (-OH) functional group at the 4th position of the pyrazole ring, while the 1-phenyl group signifies the attachment of a phenyl ring (a benzene ring) at the 1st position. 4-Hydroxy-1-phenylpyrazole is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of certain dyes and pigments. Due to its unique structure and properties, 4-hydroxy-1-phenylpyrazole has attracted interest in the field of organic chemistry and material science.

1076-60-4

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1076-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1076-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1076-60:
(6*1)+(5*0)+(4*7)+(3*6)+(2*6)+(1*0)=64
64 % 10 = 4
So 1076-60-4 is a valid CAS Registry Number.

1076-60-4SDS

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 1-phenylpyrazol-4-ol

1.2 Other means of identification

Product number -
Other names 1-Phenyl-1H-pyrazol-4-ol

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:1076-60-4 SDS

1076-60-4Downstream Products

1076-60-4Relevant academic research and scientific papers

Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives

Westaway, Susan M.,Preston, Alex G. S.,Barker, Michael D.,Brown, Fiona,Brown, Jack A.,Campbell, Matthew,Chung, Chun-Wa,Drewes, Gerard,Eagle, Robert,Garton, Neil,Gordon, Laurie,Haslam, Carl,Hayhow, Thomas G.,Humphreys, Philip G.,Joberty, Gerard,Katso, Roy,Kruidenier, Laurens,Leveridge, Melanie,Pemberton, Michelle,Rioja, Inma,Seal, Gail A.,Shipley, Tracy,Singh, Onkar,Suckling, Colin J.,Taylor, Joanna,Thomas, Pamela,Wilson, David M.,Lee, Kevin,Prinjha, Rab K.

, p. 1370 - 1387 (2016/03/05)

Following the discovery of cell penetrant pyridine-4-carboxylate inhibitors of the KDM4 (JMJD2) and KDM5 (JARID1) families of histone lysine demethylases (e.g., 1), further optimization led to the identification of non-carboxylate inhibitors derived from pyrido[3,4-d]pyrimidin-4(3H)-one. A number of exemplars such as compound 41 possess interesting activity profiles in KDM4C and KDM5C biochemical and target-specific, cellular mechanistic assays.

Hydroxylation of various molecules including heterocyclic aromatics using recombinant Escherichia coli cells expressing modified biphenyl dioxygenase genes

Misawa, Norihiko,Shindo, Kazutoshi,Takahashi, Haruko,Suenaga, Hikaru,Iguchi, Kazuo,Okazaki, Hiroshi,Harayama, Shigeaki,Furukawa, Kensuke

, p. 9605 - 9612 (2007/10/03)

Various molecules, in which heterocyclic aromatics are linked with phenyl or benzyl groups, were converted to their corresponding cis-dihydrodiols by recombinant Escherichia coli cells expressing modified biphenyl dioxygenase genes. Heterocyclic aromatic

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