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4-AMINO-2-(1-PIPERIDINYL)PYRIMIDINE-5-CARBONITRILE is a pyrimidine derivative chemical compound with the molecular formula C10H11N5. It features a six-membered nitrogen-containing ring with a piperidinyl group attached, which contributes to its unique chemical properties and potential interactions with biological targets.

90973-23-2

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90973-23-2 Usage

Uses

Used in Pharmaceutical Synthesis:
4-AMINO-2-(1-PIPERIDINYL)PYRIMIDINE-5-CARBONITRILE is used as a key intermediate in the synthesis of pharmaceutical compounds. Its ability to interact with biological targets makes it a valuable component in the development of new drugs.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-AMINO-2-(1-PIPERIDINYL)PYRIMIDINE-5-CARBONITRILE serves as a research tool for studying the structure-activity relationships of potential drug candidates. Its unique chemical structure allows researchers to explore its interactions with various biological targets and understand its potential therapeutic effects.
Used in Drug Discovery and Development:
Due to its potential to modulate the functions of biological targets, 4-AMINO-2-(1-PIPERIDINYL)PYRIMIDINE-5-CARBONITRILE is utilized in drug discovery and development processes. Its precise applications and properties may vary depending on the specific context and target of interest, making it a versatile compound in the search for novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 90973-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,7 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90973-23:
(7*9)+(6*0)+(5*9)+(4*7)+(3*3)+(2*2)+(1*3)=152
152 % 10 = 2
So 90973-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N5/c11-6-8-7-13-10(14-9(8)12)15-4-2-1-3-5-15/h7H,1-5H2,(H2,12,13,14)

90973-23-2 Well-known Company Product Price

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  • Aldrich

  • (563854)  4-Amino-2-(1-piperidinyl)pyrimidine-5-carbonitrile  97%

  • 90973-23-2

  • 563854-1G

  • 1,285.83CNY

  • Detail

90973-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-2-piperidin-1-ylpyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-amino-2-piperidin-1-yl-pyrimidine-5-carbonitrile

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 -
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More Details:90973-23-2 SDS

90973-23-2Relevant academic research and scientific papers

Facile synthesis of pyrazolo[3,4-d]pyrimidines and pyrimido[4,5-d] pyrimidin-4-one derivatives

Katiyar, Sanjay Babu,Kumar, Arun,Chauhan, Prem M. S.

, p. 2963 - 2973 (2007/10/03)

Pyrazolopyrimidine and pyrimidopyrimidine derivatives have shown a wide range of biological activities such as acting as A1 adenosine receptors, kinase insert domain receptor (KDR), Rous sarcoma oncogene (Src), epidermal growth factor receptor (EGFR), antiproliferative, dihydrofolate reductase (DHFR), antimicrobial, antifungal, and lipid peroxidation. Because of this wide range of activities, we have synthesized pyrazolo[3,4-d]pyrimidines and pyrimido[4,5-d]pyrimidin-4-one derivatives. Copyright Taylor & Francis Group, LLC.

A Convenient Synthesis of 2-Substituted 4-Amino-5-pyrimidinecarbonitriles

Schmidt, Hans-Werner,Koitz, Gerald,Junek, Hans

, p. 1305 - 1307 (2007/10/02)

Synthesis of the novel 2-halogenated 4-amino-5-pyrimidinecarbonitriles 3a,b starting from ethoxymethylenemalononitrile 1 and cyanamide is described.Nucleophilic substitution of the reactive halogen atom leads to the derivatives 5a-g,6 and 7a-h.

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