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1-methyl-5-phenyl-1H-pyrazol-3-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85485-60-5

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85485-60-5 Usage

Structure

Pyrazole derivative with a methyl group and a phenyl group attached to the pyrazole ring

Pharmacological activities

Potential antiviral, antibacterial, and anti-inflammatory properties

Use in organic synthesis

Building block for the preparation of other complex compounds

Research interest

Potential applications in drug discovery and development

Check Digit Verification of cas no

The CAS Registry Mumber 85485-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,8 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85485-60:
(7*8)+(6*5)+(5*4)+(4*8)+(3*5)+(2*6)+(1*0)=165
165 % 10 = 5
So 85485-60-5 is a valid CAS Registry Number.

85485-60-5Relevant academic research and scientific papers

CRBN LIGANDS AND USES THEREOF

-

, (2019/08/20)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of CRBN, and the treatment of CRBN-mediated disorders.

NOVEL COMPOUNDS

-

, (2016/04/20)

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C-terminal hydrolase L1 (UCHL1). The invention further relates to the use of DUB inhibitors in the treatment of cancer and other indications. Compounds of the invention include compounds having the formula (I) or a pharmaceutically acceptable salt thereof, wherein R1 to R8 are as defined herein.

Aminopyrazoles. IV. Pyrazol-3- and 5-amines from 2,3-dihaloalkanenitriles or 3-Chloroacrylonitriles and Hydrazines

Ege, Guenter,Franz, Hermann

, p. 1267 - 1273 (2007/10/02)

2,3-Dihalopropanenitriles and substituted 3-chloropropenenitriles react with hydrazines in basic solution to form either pyrazol-3-amines 4 or pyrazol-5-amines 5 or a mixture of both isomers.

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