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1-(4-CHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE is a chemical compound that belongs to the class of pyrazolo-pyrimidine derivatives. It is characterized by its 4-chlorophenyl group and the presence of an amino group on the pyrazolo-pyrimidine ring, which makes it a versatile building block for the synthesis of various biologically active molecules. 1-(4-CHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE exhibits potential for medicinal and pharmaceutical applications, particularly in drug development and cancer research.

6289-04-9

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6289-04-9 Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-CHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE is used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drug candidates targeting various diseases. Its unique chemical structure allows for the creation of a wide range of biologically active molecules with potential therapeutic applications.
Used in Cancer Research:
In the field of cancer research, 1-(4-CHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE has been studied for its potential antitumor properties. Its ability to interact with various biological targets and modulate signaling pathways makes it a promising candidate for the development of novel anticancer drugs.
Used in Drug Development:
1-(4-CHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE's potential for medicinal applications extends to drug development, where it can be utilized to create new drug candidates with improved efficacy and selectivity. Its versatility as a building block for the synthesis of biologically active molecules makes it a valuable asset in the search for new treatments for various diseases.
Overall, 1-(4-CHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINE is a promising chemical compound with a wide range of potential applications in the fields of pharmaceutical synthesis, cancer research, and drug development. Its unique structure and properties make it an attractive candidate for further investigation and development as a therapeutic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 6289-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6289-04:
(6*6)+(5*2)+(4*8)+(3*9)+(2*0)+(1*4)=109
109 % 10 = 9
So 6289-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H8ClN5/c12-7-1-3-8(4-2-7)17-11-9(5-16-17)10(13)14-6-15-11/h1-6H,(H2,13,14,15)

6289-04-9 Well-known Company Product Price

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  • Aldrich

  • (JRD0236)  1-(4-Chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine  AldrichCPR

  • 6289-04-9

  • JRD0236-1G

  • 2,575.17CNY

  • Detail

6289-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 1-(4-chlorophenyl)pyrazolo[3,4-d]pyrimidin-4-amine

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:6289-04-9 SDS

6289-04-9Relevant academic research and scientific papers

Synthesis and biological evaluation of some novel fused pyrazolopyrimidines as potential anticancer and antimicrobial agents

Abd El Razik, Heba A.,Abdel Wahab, Abeer E.

body text, p. 184 - 196 (2011/10/07)

Synthesis and evaluation of anticancer and antimicrobial activity of some novel pyrazolopyrimidines and fused pyrazolopyrimidines are reported. Twelve analogs were selected to be evaluated for their in vitro anticancer potential against a panel of three h

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