ChemicalBook--->CAS DataBase List--->133427-08-4

133427-08-4

133427-08-4 Structure

133427-08-4 Structure
IdentificationBack Directory
[Name]

IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
[CAS]

133427-08-4
[Synonyms]

Imidazo[1,2-a]pyridine-8-...
Imidazo[1,2-a]pyridine-8-carboxylicaci
8-imidazo[1,2-a]pyridinecarboxylic acid
IMidazo[1,2-a]pyridin-8-carboxylic acid
IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID
H-imidazo[1,2-a]pyridine-8-carboxylic acid
H-iMidazo[1,2-a]pyridine-8-carbo×ylic acid
IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID ISO 9001:2015 REACH
[Molecular Formula]

C8H6N2O2
[MDL Number]

MFCD06739251
[MOL File]

133427-08-4.mol
[Molecular Weight]

162.15
Chemical PropertiesBack Directory
[density ]

1.41
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

-0.61±0.41(Predicted)
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P271-P261-P280
[Hazard Codes ]

Xn
[Risk Statements ]

22-43
[Safety Statements ]

36/37
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID(133427-08-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Aminonicotinic acid

5345-47-1

Bromoacetaldehyde dimethyl acetal

7252-83-7

IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID

133427-08-4

General procedure for the synthesis of imidazo[1,2-a]pyridine-8-carboxylic acid from 2-aminonicotinic acid and 2-bromo-1,1-dimethoxyethane: To a suspension of 2-aminonicotinic acid (0.69 g, 5.00 mmol) in acetonitrile (20 mL) was added 2-bromo-1,1-dimethoxyethane (0.59 mL, 5.00 mmol). The resulting mixture was heated to 150 °C in a microwave reactor and kept for 2 hours. After completion of the reaction, the precipitate was collected by filtration and washed sequentially with acetonitrile and hexane to afford imidazo[1,2-a]pyridine-8-carboxylic acid (0.924 g) as a gray solid.

[References]

[1] Patent: WO2009/23253, 2009, A2. Location in patent: Page/Page column 52
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 5, p. 1870 - 1873
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