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CAS 5536-40-3

:

(2,6-dimethyl-4-oxo-1,4-dihydropyrimidin-5-yl)acetic acid

Description:
(2,6-Dimethyl-4-oxo-1,4-dihydropyrimidin-5-yl)acetic acid, with the CAS number 5536-40-3, is a chemical compound that belongs to the class of dihydropyrimidines. This substance features a pyrimidine ring structure that is substituted at the 2 and 6 positions with methyl groups, contributing to its unique properties. The presence of a keto group at the 4-position and a carboxylic acid functional group at the 5-position enhances its reactivity and solubility in polar solvents. It is typically a solid at room temperature and may exhibit moderate stability under standard conditions. The compound is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anti-inflammatory properties. Its synthesis often involves multi-step organic reactions, and it can be characterized using techniques such as NMR spectroscopy and mass spectrometry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices.
Formula:C8H10N2O3
InChI:InChI=1/C8H10N2O3/c1-4-6(3-7(11)12)8(13)10-5(2)9-4/h3H2,1-2H3,(H,11,12)(H,9,10,13)
SMILES:Cc1c(CC(=O)O)c(nc(C)n1)O
Synonyms:
  • (4-Hydroxy-2,6-dimethylpyrimidin-5-yl)acetic acid
  • 5-Pyrimidineacetic Acid, 1,4-Dihydro-2,6-Dimethyl-4-Oxo-
  • 5-Pyrimidineacetic Acid, 4-Hydroxy-2,6-Dimethyl-
  • (2,6-Dimethyl-4-oxo-1,4-dihydropyrimidin-5-yl)acetic acid
  • (4-Hydroxy-2,6-dimethyl-pyrimidin-5-yl)-aceticaci
  • (4-HYDROXY-2,6-DIMETHYL-PYRIMIDIN-5-YL)-ACETIC ACID ISO 9001：2015 REACH
  • 2-(2,4-dimethyl-6-oxo-1,6-dihydropyrimidin-5-yl)acetic acid
  • 5-Pyrimidineacetic acid, 1,6-dihydro-2,4-dimethyl-6-oxo-
  • (4-hydroxy-2,6-dimethylpyrimidin-5-yl)acetic acid(SALTDATA: FREE)
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