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2-(5-AMINO-1H-PYRAZOL-3-YL)-PHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10523-64-5

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10523-64-5 Usage

Molar mass

184.19 g/mol

Structure

Phenolic derivative with a pyrazole ring and an amino group attached

Usage

Commonly used in pharmaceutical research

Potential applications

Drug development

Involvement in biological processes

Unknown, but has shown potential in the treatment of certain diseases

Significance

Interesting target for further study and potential use in medicinal applications

Check Digit Verification of cas no

The CAS Registry Mumber 10523-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10523-64:
(7*1)+(6*0)+(5*5)+(4*2)+(3*3)+(2*6)+(1*4)=65
65 % 10 = 5
So 10523-64-5 is a valid CAS Registry Number.

10523-64-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(5-amino-1,2-dihydropyrazol-3-ylidene)cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 3-o-Oxyphenyl-5-amino-pyrazol

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:10523-64-5 SDS

10523-64-5Downstream Products

10523-64-5Relevant academic research and scientific papers

Pyrazolotriazines as inhibitors of nucleases

-

Paragraph 0122; 0123; 0124; 0125; 0126; 0127; 0176-0179, (2016/01/12)

The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3 and R4 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.

A Convenient and Practical Synthesis of Aminopyrazoles

Mitchell, David,Luo, Yumei,Mcnulty, Lu Anne M.,Buser, Jonas Y.,Mcfarland, Adam D.

, p. 235 - 241 (2015/05/05)

A selective methodology for preparing highly substituted aminopyrazoles has been demonstrated. Starting with an acetophenol core, the corresponding substituted isoxazole is prepared in two steps. The isoxazole is transformed into a benzopyran. Alkylation

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