Imidazo[1,5-a]pyridine-7-carboxylic acid

Basic Information

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CAS Number

588720-29-0

Molecular Formula

C8H6N2O2

Molecular Weight

162.15 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Fine Chemicals Dyes and Pigments Organic Dyes

Basic Physical Properties

Density

1.41

Refractive Index

1.676

SMILES

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C1=CN2C=NC=C2C=C1C(=O)O

InChI

InChI=1S/C8H6N2O2/c11-8(12)6-1-2-10-5-9-4-7(10)3-6/h1-5H,(H,11,12)

InChIKey

GMBMIWBXIHLWDP-UHFFFAOYSA-N

LogP

1.0324999999999998

Topological Polar Surface Area

54.599999999999994 Å²

Hydrogen Bond Donor/Acceptor

1 / 4

Complexity

196

Synonyms & References

English

FT-0647202
Imidazo[1,5-a]pyridine-7-carboxylic acid (9CI)
EN300-111394
Imidazo[1 pound not5-a]pyridine-7-carboxylicacid
J-521513
AM20061353
588720-29-0
SY105104
GMBMIWBXIHLWDP-UHFFFAOYSA-N
Imidazo[1,5-a]pyridine-7-carboxylicacid
AKOS015919907
MFCD11870763
Z1255443427
IMIDAZO[1,5-A]PYRIDINE-7-CARBOXYLIC ACID
FS-2947
DTXSID30478213
A8305
CS-0082360
SCHEMBL1759118
Imidazo[1,5-a]pyridine-7-carboxylic acid
H-imidazo[1,5-a]pyridine-7-carboxylic acid
PubChem23099
VP13646
RP22500
AB0025688
W7186
ST24030776
imidazo[1,5-a]pyridine-7-carboxylic acid

MDL Number

MFCD11870763

Customs Code

2933990090

FAQ

What are the physical and chemical properties of Imidazo[1,5-a]pyridine-7-carboxylic acid (CAS: 588720-29-0)?

Imidazo[1,5-a]pyridine-7-carboxylic acid is a crystalline solid with a molecular weight of approximately 239.24 g/mol. It is slightly soluble in water and solvents like ethanol and methanol. The compound is chemically reactive, particularly towards nucleophilic substitution and condensation reactions.

How is Imidazo[1,5-a]pyridine-7-carboxylic acid (CAS: 588720-29-0) typically synthesized?

Imidazo[1,5-a]pyridine-7-carboxylic acid can be synthesized via the condensation of 2-acetylpyridine with 1H-imidazole followed by the removal of the acetyl group. The reaction typically uses thionyl chloride for acetylation and a catalytic amount of pyridine for deacetylation.

What industries use Imidazo[1,5-a]pyridine-7-carboxylic acid (CAS: 588720-29-0)?

Imidazo[1,5-a]pyridine-7-carboxylic acid finds applications in pharmaceuticals, where it serves as a precursor for drug synthesis, and in the development of advanced polymers and sensors. It also has potential uses in the semiconductor industry for doping purposes.

What precautions should be taken when handling Imidazo[1,5-a]pyridine-7-carboxylic acid (CAS: 588720-29-0)?

Handling Imidazo[1,5-a]pyridine-7-carboxylic acid requires caution as it is a reactive compound. Always wear appropriate personal protective equipment (PPE) including gloves, goggles, and a lab coat. Work in a well-ventilated fume hood or a well-ventilated area. Follow standard laboratory safety protocols and consult the Safety Data Sheet (SDS) for specific handling instructions.