ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Pyrimidines > Aminopyrimidine > 5-Amino-4-methylpyrimidine
5-Amino-4-methylpyrimidine
5-Amino-4-methylpyrimidine Basic information
- Product Name:
- 5-Amino-4-methylpyrimidine
- Synonyms:
-
- 5-AMINO-4-METHYLPYRIMIDINE
- 5-AMIO-4-METHYLPYRIMIDINE
- 5-Pyrimidinamine, 4-methyl- (9CI)
- 5-Pyrimidinamine, 4-methyl
- 4-Methylpyrimidin-5-amine
- 4-Methyl-5-pyrimidinamine
- (4-methylpyrimidin-5-yl)amine
- Pyrimidine, 5-amino-4-methyl-
- CAS:
- 3438-61-7
- MF:
- C5H7N3
- MW:
- 109.13
- Product Categories:
-
- Heterocycle-Pyrimidine series
- PYRIMIDINE
- Mol File:
- 3438-61-7.mol
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5-Amino-4-methylpyrimidine Chemical Properties
- Melting point:
- 151-151.5 °C
- Boiling point:
- 246.8±20.0 °C(Predicted)
- Density
- 1.155±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 3.21±0.16(Predicted)
- Appearance
- White to yellow Solid
- InChI
- InChI=1S/C5H7N3/c1-4-5(6)2-7-3-8-4/h2-3H,6H2,1H3
- InChIKey
- DQNDDUOCVSWTOW-UHFFFAOYSA-N
- SMILES
- C1=NC=C(N)C(C)=N1
- CAS DataBase Reference
- 3438-61-7(CAS DataBase Reference)
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5-Amino-4-methylpyrimidine Usage And Synthesis
Uses
5-Amino-4-methylpyrimidine is a pharmaceutical intermediate compound. Its structural features include a methyl group and an amino group attached to the 4th and 5th positions, respectively, on the pyrimidine ring. This substance can be used in the preparation of anticancer inhibitory compounds.
Synthesis
When 5-amino-2,4- dichloro-6-methylpyrimidine was hydrogenated over 10% palladium-on-charcoal in the presence of excess magnesium oxide a 31 % yield of 5-amino-4-methylpyrimidine was obtained[1].
References
[1] C. G. Overberger, W. J. E., Irving C. Kogon. (1954). Derivatives of 5-Amino-4-methylpyrimidine. Journal of the American Chemical Society, 76 7, 1953–1954. https://doi.org/10.1021/ja01636a069
5-Amino-4-methylpyrimidineSupplier
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5-Amino-4-methylpyrimidine(3438-61-7)Related Product Information
- 2-Amino-4-(trifluoromethyl)pyrimidine
- 2,4-Dichloro-6-methyl-5-nitropyrimidine
- 5-Nitro-6-methyluracil
- 5-AMINO-2,4-DIHYDROXY-6-METHYLPYRIMIDINE
- N-(5-IODO-3-METHYL-PYRIDIN-2-YL)-2,2-DIMETHYL-PROPIONAMIDE
- 2-Chloro-6-methylpyrimidin-4-ylamine
- 2-AMINO-4-METHYL-PYRIMIDINE-5-CARBOXYLIC ACID
- 4-AMINO-2-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBONITRILE
- 2-(TRIFLUOROMETHYL)PYRIMIDIN-5-AMINE
- 2-(TRIFLUOROMETHYL)PYRIMIDIN-4-AMINE
- 4-Pyrimidinamine, 2-(chloromethyl)- (9CI)
- 2-Chloro-6-(trifluoromethyl)pyrimidin-4-amine
- 4,6-dimethyl-2-aminopyrimidine
- 5-Amino-4,6-dichloro-2-methylpyrimidine
- 4-AMINO-2-METHYL-PYRIMIDINE-5-CARBOXYLIC ACID
- 5-(AMINOMETHYL)-2-METHYLPYRIMIDIN-4-AMINE
- 5-Amino-2,6-dimethylpyrimidine
- 4-AMINO-2-METHYLPYRIMIDINE-5-CARBONITRILE