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2-Amino-4-methylpyrimidine

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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
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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
pka
pK1: 4.11(+1) (20°C)
color 
Off-white to light brown
BRN 
108506
CAS DataBase Reference
108-52-1(CAS DataBase Reference)
NIST Chemistry Reference
2-Amino-4-methylpyrimidine(108-52-1)
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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

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2-Amino-4-methylpyrimidine Usage And Synthesis

Chemical Properties

OFF-WHITE TO LIGHT BROWN CRYSTALLINE POWDER

Uses

2-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.

Definition

ChEBI: 2-Amino-4-methylpyrimidine is an aminopyrimidine.

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 3526, 1951 DOI: 10.1021/ja01151a529

Purification Methods

Crystallise 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.]

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