2-Amino-4-methylpyrimidine

2-Amino-4-methylpyrimidine
  • CAS No.:108-52-1
Other grades of this product :
2-Amino-4-methylpyrimidine Basic information
Product Name:2-Amino-4-methylpyrimidine
Synonyms:TIMTEC-BB SBB004343;2-AMINO-4-METHYLPYRIMIDINE FOR SYNTHESIS;2-amino-4-methyl-pyrimidin;2-Pyrimidinamine, 4-methyl-;4-Methyl-2-pyrimidinamine;6-Methyl-2-pyrimidinamine;Pyrimidine, 2-amino-4-methyl-;2-AMINO-4-METHYLPYRIMIDINE
CAS:108-52-1
MF:C5H7N3
MW:109.13
EINECS:203-591-5
Product Categories:Heterocycle-Pyrimidine series;Building Blocks;PYRIMIDINE;Pyridines, Pyrimidines, Purines and Pteredines;Heterocyclic Building Blocks;Pyrimidines
Mol File:108-52-1.mol
2-Amino-4-methylpyrimidine Chemical Properties
Melting point 158-160 °C(lit.)
Boiling point 194.6°C (rough estimate)
density 1 g/cm3
refractive index 1.5340 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Crystalline Powder
pkapK1: 4.11(+1) (20°C)
color Off-white to light brown
BRN 108506
CAS DataBase Reference108-52-1(CAS DataBase Reference)
NIST Chemistry Reference2-Amino-4-methylpyrimidine(108-52-1)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS UV6485000
Hazard Note Irritant
HS Code 29335990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
2-Amino-4-methylpyrimidine Usage And Synthesis
Chemical PropertiesOFF-WHITE TO LIGHT BROWN CRYSTALLINE POWDER
Uses2-Amino-4-methylpyrimidine is a compound involved in a study about carbonylation as a key reaction in anaerobic acetone activation by Desulfococcus biacutus. 2-Amino-4-methylpyrimidine is formed as the product of a reaction between acetoacetaldehyde and guanidine.
Synthesis Reference(s)Journal of the American Chemical Society, 73, p. 3526, 1951 DOI: 10.1021/ja01151a529
Purification MethodsCrystallise the pyrimidine from H2O or EtOH and sublime it in a vacuum. The picrate crystallises from EtOH and has m 235-236o(dec). [Beilstein 24 H 84, 25 III/IV 2152.]
2-Amino-4-methylpyrimidine Preparation Products And Raw materials

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