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2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid is a complex organic compound with the molecular formula C11H10N2O4. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring containing four carbon atoms and two nitrogen atoms. The compound features a phenyl group attached to the pyrimidine ring, and it has two oxygen atoms (keto groups) at the 2nd and 6th positions, as well as a carboxylic acid group at the 4th position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly those involving pyrimidine-based structures. Its unique structure and properties make it an interesting target for researchers in the field of organic chemistry and drug development.

723-76-2

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723-76-2 Usage

Molecular Structure

2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid has a complex molecular structure, which is characterized by a fusion of a phenyl group and a carboxylic acid functional group within a pyrimidine derivative framework.

Class

This chemical compound belongs to the class of pyrimidine derivatives, which are heterocyclic organic compounds with a six-membered ring structure containing four carbon atoms and two nitrogen atoms.

Functional Groups

The presence of a phenyl group (an aromatic ring with a hydrogen atom) and a carboxylic acid functional group (a carbonyl group bonded to a hydroxyl group) are key features of 2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid.

Biological Activity

2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid is known for its potential biological activity, which has led to its study for various therapeutic applications.

Anti-bacterial Properties

2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid has been studied for its ability to inhibit the growth of bacteria, making it a potential candidate for the development of new antibiotics.

Anti-inflammatory Properties

2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid has also been investigated for its potential to reduce inflammation, which could be useful in the treatment of various inflammatory conditions.

Pharmaceutical Synthesis

2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid is used in the synthesis of various pharmaceuticals and organic compounds, making it an important building block in the development of new drugs and therapies.

Versatility

The unique structure and properties of 2,6-dioxo-1-phenyl-1,2,3,6-tetrahydro-pyrimidine-4-carboxylic acid make it a versatile chemical, applicable in a wide range of research areas within medicinal and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 723-76-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 723-76:
(5*7)+(4*2)+(3*3)+(2*7)+(1*6)=72
72 % 10 = 2
So 723-76-2 is a valid CAS Registry Number.
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