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Home/Compounds/Pharmaceutical Intermediate/2-Butyl-1,4-dihydro-6-methyl-4-oxo-5-pyrimidineacetic acid ethyl ester
C13H20N2O3
252.31 g/mol
Pharmaceutical Intermediate

Ethyl 2-(2-butyl-4-hydroxy-6-methylpyrimidin-5-yl)acetate

CAS503155-65-5
Category
Pharmaceutical Intermediate
Compound Class
Heterocycle
Primary Use
Pharmaceutical Intermediate

This compound is an ethyl ester derivative of a substituted pyrimidinone. It is primarily used as a pharmaceutical intermediate in the synthesis of other compounds.

pharmaceutical intermediate

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

SimilarStructure SimilarSimilarity 0.73

2-Butyl-1,6-dihydro-4-methyl-6-oxo-5-pyrimidineacetic acid

CAS1315478-16-0

pharmaceutical intermediate

SimilarStructure SimilarSimilarity 0.72

2-Butyl-1,6-dihydro-N,N,4-trimethyl-6-oxo-5-pyrimidineacetamide

CAS1315478-13-7

pharmaceutical intermediate

ReferenceSame Category

2-Butyl-1,6-dihydro-N,N,4-trimethyl-6-oxo-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-5-pyrimidineacetamide

CAS503155-67-7

pharmaceutical intermediate

ReferenceSame Category

N-(3-Aminopropyl)-imidazole

CAS5036-48-6

pharmaceutical intermediate

ReferenceSame Category

1-(4-Methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-yl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylic acid ethyl ester

CAS503614-91-3

pharmaceutical intermediate

ReferenceSame Category

5,6-Dihydro-3-(4-morpholinyl)-1-(4-nitrophenyl)-2(1H)-pyridinone

CAS503615-03-0

pharmaceutical intermediate

Referencesame scaffold

2-AMINO-4,6-DIHYDROXY-5-NITROSOPYRIMIDINE

CAS55482-22-9

research compound

Referencesame scaffold

2,4,5-Triamino-6-hydroxypyrimidine sulfate

CAS35011-47-3

pharmaceutical intermediate

Identifiers
IUPAC Name

ethyl 2-(2-butyl-4-methyl-6-oxo-1H-pyrimidin-5-yl)acetate

InChIKey

PUNKBDMMPFKQMA-UHFFFAOYSA-N

SMILES

CCCCC1=NC(=C(C(=O)N1)CC(=O)OCC)C

Synonyms (6)

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