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[1,2,4]Triazolo[1,5-a]pyrimidin-2-amine, also known as TPA, is a chemical compound characterized by its triazolopyrimidine structure. It is recognized for its potential in pharmaceutical compound synthesis and heterocyclic derivative formation, making it a valuable building block in drug development and medicinal chemistry. TPA's ability to interact with biological targets and modulate their activity has garnered significant interest, positioning it as a key compound in the realms of chemical and pharmaceutical research.

13223-53-5

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13223-53-5 Usage

Uses

Used in Pharmaceutical Compound Synthesis:
[1,2,4]Triazolo[1,5-a]pyrimidin-2-amine is used as a building block for the synthesis of various pharmaceutical compounds. Its structural properties allow for the creation of a wide range of heterocyclic derivatives, contributing to the development of novel drugs with potential therapeutic applications.
Used in Drug Development:
TPA is utilized as a key component in drug development due to its ability to interact with biological targets. This interaction enables the modulation of target activity, which can lead to the creation of new therapeutic agents with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [1,2,4]Triazolo[1,5-a]pyrimidin-2-amine is employed as a reagent for the preparation of compounds with biological and pharmacological activities. Its diverse potential biological and pharmacological properties make it an important compound for research and development in this area.
Used in Organic Chemistry:
TPA is also used as a reagent in organic chemistry, particularly in the preparation of compounds with potential applications in the pharmaceutical and chemical industries. Its unique structure and properties facilitate the synthesis of a variety of organic compounds with specific biological and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 13223-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13223-53:
(7*1)+(6*3)+(5*2)+(4*2)+(3*3)+(2*5)+(1*3)=65
65 % 10 = 5
So 13223-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N5/c6-4-8-5-7-2-1-3-10(5)9-4/h1-3H,(H2,6,9)

13223-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,2,4]Triazolo[1,5-a]pyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-s-triazolo<2,3-a>pyrimidin

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:13223-53-5 SDS

13223-53-5Downstream Products

13223-53-5Relevant academic research and scientific papers

Cyanoamino Compounds in Synthesis Syntheses of Some Heterocycles

Vercek, Bojan,Ogorevc, Bozidar,,Stanovnik, Branko,Tisler, Miha

, p. 789 - 798 (2007/10/02)

Transformations of some heterocyclic cyanoamino compounds leading to various heterocyclic systems are described. s-Triazolo(1,5-a)azines are obtained either in a direct synthetic approach or via the substituted aminotetrazoles, substituted 3-amino-5-oxo-1,2,4-oxadiazolines, and from N-ethoxycarbonyl N'-heteroaryl thioureas or N-heteroaryl N'-hydroxyguanidine.The cyanoamino group reacts also with o-difunctional benzenes to give the corresponding substituted derivatives of benzimidazole, benzoxazole or benzothiazole. - Keywords: Cyclization with N-N bond formation; Heterocyclic compounds; Rearrangements

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