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2-Amino-4,6-dimethylpyridine

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2-Amino-4,6-dimethylpyridine Basic information

Product Name:
2-Amino-4,6-dimethylpyridine
Synonyms:
  • Pyridine, 2-amino-4,6-dimethyl-
  • 2-amino-4,6-dimethylpyridine (6-amino-2,4,-lutidine)
  • 2,4-Dimethyl-6-aminopyridine
  • 6-Amino-2,4dimethylpyridine
  • 4,6-dimethyl-2-pyridylamine
  • 6-AMINO-2,4-LUTIDINE 98+%
  • 6-Amino-2,4-lutidine, 4,6-Dimethylpyridin-2-amine
  • 2-AMino-4,6-diMehtylpyridine
CAS:
5407-87-4
MF:
C7H10N2
MW:
122.17
EINECS:
226-470-9
Product Categories:
  • Heterocycle-Pyridine series
  • Amines
  • Pyridine series
  • Pyridines
  • Pyridine
Mol File:
5407-87-4.mol
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2-Amino-4,6-dimethylpyridine Chemical Properties

Melting point:
63-64 °C (lit.)
Boiling point:
235 °C (lit.)
Density 
1.0959 (rough estimate)
refractive index 
1.6100 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
7.62±0.35(Predicted)
form 
Crystalline Powder
color 
White to light brown
InChI
InChI=1S/C7H10N2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3,(H2,8,9)
InChIKey
BRBUBVKGJRPRRD-UHFFFAOYSA-N
SMILES
C1(N)=NC(C)=CC(C)=C1
CAS DataBase Reference
5407-87-4(CAS DataBase Reference)
NIST Chemistry Reference
2-Pyridinamine, 4,6-dimethyl-(5407-87-4)
EPA Substance Registry System
2-Pyridinamine, 4,6-dimethyl- (5407-87-4)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-37/39
WGK Germany 
3
RTECS 
US1818000
Hazard Note 
Irritant
HS Code 
2933399990

MSDS

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2-Amino-4,6-dimethylpyridine Usage And Synthesis

Chemical Properties

White to off-white crystalline

Uses

Organic intermediate.

Uses

2-Amino-4,6-dimethylpyridine, can be used in the synthesis of various chemical compounds having therapeutic activity, such as in preparation of quinoline and quinoxaline compounds having anticancer activity.

Application

2-Amino-4,6-dimethylpyridine is a nonsteroidal anti-inflammatory drug that inhibits the production of prostaglandins and leukotrienes. 2-Amino-4,6-dimethylpyridine binds to the cyclooxygenase enzyme and blocks its conversion of arachidonic acid to prostaglandin H2. This compound has been shown to have potent inhibitory effects against Leishmania, with high values in reactive compounds. The molecular modeling of this compound shows that it has an unpaired amino function and an amide.

Purification Methods

Recrystallise this base from hexane, ether/pet ether or *benzene. Residual *benzene is removed over paraffin-wax chips in an evacuated desiccator. The dipicrate crystallises from EtOH and has m 205-207o(dec). [Beilstein 22 III/IV 4210.]

2-Amino-4,6-dimethylpyridine Preparation Products And Raw materials

Raw materials

2-Amino-4,6-dimethylpyridineSupplier

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