2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE

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Products Intro: Product Name:2-Methyloxazolo[4,5-b]pyridine
CAS:86467-39-2
Purity:99% Package:100kg;1.6USD|10kg;6.6USD|1kg;9.6USD
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Products Intro: Product Name:2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE
CAS:86467-39-2
Purity:NLT 98% Package:1G;1KG;100KG
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Products Intro: Product Name:2-Methyloxazolo[4,5-b]pyridine
CAS:86467-39-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-07598
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Products Intro: Product Name:2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE
CAS:84467-39-2
Purity:99% Package:1g;2USD
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Products Intro: Product Name:2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE
CAS:86467-39-2
Purity:NLT 98% Package:1G;1KG;100KG Remarks:CF12082

2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE manufacturers

2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE Basic information
Product Name:2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE
Synonyms:2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE;2-Methyloxazolo[4,5-b]pyridine;Oxazolo[4,5-b]pyridine, 2-methyl-
CAS:86467-39-2
MF:C7H6N2O
MW:134.14
EINECS:
Product Categories:Heterocycle-Pyridine series;Fused Ring Systems
Mol File:86467-39-2.mol
2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE Structure
2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE Chemical Properties
Melting point 74 °C(Solv: ligroine (8032-32-4))
Boiling point 214.3±13.0 °C(Predicted)
density 1.229±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
pka0.22±0.50(Predicted)
color Yellow
Safety Information
HS Code 2933399990
MSDS Information
2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE Usage And Synthesis
Synthesis
2-Amino-3-hydroxypyridine

16867-03-1

Triethyl orthoacetate

78-39-7

2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE

86467-39-2

General procedure for the synthesis of 2-methyloxazolo[4,5-B]pyridine from 2-amino-3-hydroxypyridine and triethyl orthoacetate: 80 mL of triethyl orthoacetate was added to 15 g (136 mmol) of 2-amino-3-hydroxypyridine, followed by the addition of a catalytic amount of p-toluenesulfonic acid. The reaction mixture was stirred at 120 °C for 4 hours. After completion of the reaction, the reaction mixture was cooled and triethylamine was added to neutralize p-toluenesulfonic acid in the reaction system. Subsequently, the solvent was removed by distillation under reduced pressure using a rotary evaporator. The crude product was purified by silica gel column chromatography to afford 12.0 g of the target product 2-methyloxazolo[4,5-B]pyridine in 65.8% yield.

References[1] Monatshefte fur Chemie, 2011, vol. 142, # 1, p. 87 - 91
[2] Heterocycles, 1995, vol. 41, # 3, p. 477 - 486
[3] Monatshefte fur Chemie, 2007, vol. 138, # 7, p. 663 - 667
[4] Patent: US2009/247736, 2009, A1. Location in patent: Page/Page column 13
[5] Tetrahedron Letters, 1990, vol. 31, # 8, p. 1155 - 1156
2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE Preparation Products And Raw materials
Raw materials2-Amino-3-hydroxypyridine-->Triethyl orthoacetate
Tag:2-METHYL[1,3]OXAZOLO[4,5-B]PYRIDINE(86467-39-2) Related Product Information
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