871266-84-1 Usage
Description
(7-CHLOROTHIAZOLO[5,4-D]PYRIMIDIN-2-YL)-PYRIDIN-3-YL-AMINE is a complex chemical compound characterized by its thiazolopyrimidine core, pyridine group, and amine functional group. (7-CHLOROTHIAZOLO[5,4-D]PYRIMIDIN-2-YL)-PYRIDIN-3-YL-AMINE holds potential in medicinal chemistry, particularly for the development of novel pharmaceuticals. The presence of the thiazolopyrimidine core indicates that it may exhibit biological activity, possibly as a kinase inhibitor or as a ligand for a specific biological target. Its structural features render it a potentially valuable tool for the creation of new drugs and chemical probes in biological research.
Uses
Used in Pharmaceutical Development:
(7-CHLOROTHIAZOLO[5,4-D]PYRIMIDIN-2-YL)-PYRIDIN-3-YL-AMINE is used as a compound in pharmaceutical development for its potential as a kinase inhibitor or a ligand for specific biological targets. Its unique structure and functional groups make it a promising candidate for the creation of new drugs and chemical probes.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (7-CHLOROTHIAZOLO[5,4-D]PYRIMIDIN-2-YL)-PYRIDIN-3-YL-AMINE is used as a research tool to explore its potential biological activities and interactions with various biological targets. This can lead to the development of new therapeutic agents and a better understanding of biological processes.
Used in Drug Design and Optimization:
(7-CHLOROTHIAZOLO[5,4-D]PYRIMIDIN-2-YL)-PYRIDIN-3-YL-AMINE is utilized in drug design and optimization processes, where its structural features can be exploited to create more effective and targeted pharmaceuticals. Its potential as a kinase inhibitor or ligand makes it a valuable starting point for designing drugs with improved efficacy and selectivity.
Used in Biological Research:
In biological research, (7-CHLOROTHIAZOLO[5,4-D]PYRIMIDIN-2-YL)-PYRIDIN-3-YL-AMINE serves as a chemical probe to investigate the mechanisms of various biological processes and pathways. Its interaction with specific targets can provide insights into the development of new therapeutic strategies and the understanding of disease mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 871266-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,2,6 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 871266-84:
(8*8)+(7*7)+(6*1)+(5*2)+(4*6)+(3*6)+(2*8)+(1*4)=191
191 % 10 = 1
So 871266-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6ClN5S/c11-8-7-9(14-5-13-8)17-10(16-7)15-6-2-1-3-12-4-6/h1-5H,(H,15,16)
871266-84-1Relevant articles and documents
Single-step syntheses of 2-amino-7-chlorothiazolo[5,4-d]pyrimidines: Intermediates for bivalent thiazolopyrimidines
Liu, Jian,Patch, Raymond J.,Schubert, Carsten,Player, Mark R.
, p. 10194 - 10197 (2007/10/03)
A single-step process for the preparation of 2-amino-7-chlorothiazolo[5,4- d]pyrimidines, 2, was achieved by the reaction of the commercially available 4,6-dichloro-5-aminopyrimidine 1 with isothiocyanates. This mild reaction accommodates a variety of fun
