22434-15-7

Basic information

• Product Name: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-cyclohexen-1-yl)-5-ethyl-1-methyl-, (R)-
• CAS NO: 22434-15-7
• Molecular Formula: C13H18N2O3
• Molecular Weight: 250.298
• Mol File: 22434-15-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-cyclohexen-1-yl)-5-ethyl-1-methyl-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-cyclohexen-1-yl)-5-ethyl-1-methyl-, (R)-(22434-15-7)
• EPA Substance Registry System: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-cyclohexen-1-yl)-5-ethyl-1-methyl-, (R)-(22434-15-7)

Safety Data

• Hazardous Substances Data: 22434-15-7(Hazardous Substances Data)

Usage

Main properties and specific content of 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-cyclohexen-1-yl)-5-ethyl-1-methyl-, (R)-

This compound is composed of 12 carbon atoms, 14 hydrogen atoms, 2 nitrogen atoms, and 3 oxygen atoms.

Stereoisomer

(R)-
The compound is a specific stereoisomer, which means it has a unique arrangement of atoms in space.

Pyrimidinetrione derivative

It is a derivative of the parent compound pyrimidinetrione, which is a heterocyclic compound with three carbonyl groups.

Cyclohexenyl and ethyl groups attached to nitrogen atoms

The compound has a cyclohexenyl group (a six-membered ring with a double bond) and an ethyl group (a two-carbon chain) attached to the nitrogen atoms.

Pharmaceutical industry

The compound may have potential uses in the development of new drugs due to its unique structure and properties.

Agrochemicals

It could be used in the development of new pesticides or other agricultural chemicals.

Materials science

The compound may have potential applications in the development of new materials with specific properties.

Stereochemistry influence

The stereochemistry of the compound may affect its interactions with biological systems or chemical reactions, making it an important molecule for further research and development.

Upstream product

• 138548-32-0 5-(1-cyclohexenyl)-1,3-bis(propionyloxymethyl)-5-ethylbarbital 

Relevant articles and documents

Lipase-catalyzed Enantioselective Hydrolysis of N-Acyloxymethyl Groups in Organic Solvent: Syntheses of Chiral 5,5-Disubstituted 1-Methylbarbiturates

Chiral 5,5-disubstituted N-acyloxymethylbarbiturates have been obtained in 40-99percent optical yields by lipase-catalyzed hydrolyses of 5,5-disubstituted bisacyloxymethylbarbiturates in H2O-saturated diisopropyl ether.These chiral barbiturates were readi