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1-Propanone, 1-(2-amino-4-pyridinyl)-(9CI), also known as 2-amino-4-(1-oxopropyl)pyridine, is an organic compound with the chemical formula C8H10N2O. It is a derivative of propanone (acetone) with a 2-amino-4-pyridinyl group attached to the carbonyl carbon. 1-Propanone,1-(2-amino-4-pyridinyl)-(9CI) is characterized by its amine and pyridine functional groups, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals and agrochemicals. The presence of the carbonyl group in the propanone moiety allows for further chemical modifications, while the amino and pyridine groups can participate in various reactions, such as acylation, alkylation, and oxidation. Overall, 1-Propanone, 1-(2-amino-4-pyridinyl)-(9CI) is a versatile organic molecule with potential applications in the synthesis of more complex compounds and as a building block in the development of new drugs and materials.

87121-56-0

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87121-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87121-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,2 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87121-56:
(7*8)+(6*7)+(5*1)+(4*2)+(3*1)+(2*5)+(1*6)=130
130 % 10 = 0
So 87121-56-0 is a valid CAS Registry Number.

87121-56-0Downstream Products

87121-56-0Relevant academic research and scientific papers

The synthesis of 2-amino-4-(4-imidazolyl)pyridines

LaMattina

, p. 533 - 538 (2007/10/02)

A general synthetic scheme for the preparation of 2-amino-4-(4-imidazolyl)pyridines, potential histamine H2 antagonists, is described. The synthesis is based on the Neber rearrangement of 1-(4-pyridyl)-l-alkanone oxime O-tosylates to the appropriate α-aminoketones or α-aminoketals, which are then converted to the corresponding imidazoles. The reaction of Grignard reagents with 2-chloroisonicotinonitrile, as well as nucleophilic displacement of chloride by amines on 2-chloroisonicotinonitrile and derivatives, are discussed in relation to the preparation of the ketone intermediates.

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