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5-(dimethylphosphoryl)nicotinic acid, also known as 5-dimethylphosphoryl-3-pyridinecarboxylic acid, is a chemical compound with the molecular formula C8H10NO5P. It is a derivative of nicotinic acid, which is a form of vitamin B3. 5-(dimethylphosphoryl)nicotinic acid features a dimethylphosphoryl group attached to the 5-position of the nicotinic acid structure. It is an organophosphorus compound, which means it contains carbon-phosphorus bonds. Such compounds are significant in various fields, including pharmaceuticals and agrochemicals, due to their potential biological activities and applications. The specific properties and uses of 5-(dimethylphosphoryl)nicotinic acid would depend on its chemical structure and the context in which it is applied.

2361963-14-4

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2361963-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2361963-14-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,3,6,1,9,6 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2361963-14:
(9*2)+(8*3)+(7*6)+(6*1)+(5*9)+(4*6)+(3*3)+(2*1)+(1*4)=174
174 % 10 = 4
So 2361963-14-4 is a valid CAS Registry Number.

2361963-14-4Downstream Products

2361963-14-4Relevant academic research and scientific papers

Phosphine Oxides (-POMe2) for Medicinal Chemistry: Synthesis, Properties, and Applications

Stambirskyi, Maksym V.,Kostiuk, Tetiana,Sirobaba, Serhii I.,Rudnichenko, Alexander,Titikaiev, Dmytro L.,Dmytriv, Yurii V.,Kuznietsova, Halyna,Pishel, Iryna,Borysko, Petro,Mykhailiuk, Pavel K.

, p. 12783 - 12801 (2021/09/18)

A general practical approach to hetero(aromatic) and aliphatic P(O)Me2-substituted derivatives is elaborated. The key synthetic step was a [Pd]-mediated C-P coupling of (hetero)aryl bromides/iodides with HP(O)Me2. The P(O)Me2 substituent was shown to dramatically increase solubility and decrease lipophilicity of organic compounds. This tactic was used to improve the solubility of the antihypertensive drug prazosin without affecting its biological profile.

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