Cas no 97640-15-8 (3H-Imidazo[4,5-b]pyridine-2-carboxylic acid)

3H-Imidazo[4,5-b]pyridine-2-carboxylic acid structure
97640-15-8 structure
Product Name:3H-Imidazo[4,5-b]pyridine-2-carboxylic acid
CAS No:97640-15-8
MF:C7H5N3O2
MW:163.133500814438
MDL:MFCD05721719
CID:1039406
PubChem ID:22610019
Update Time:2024-10-25

3H-Imidazo[4,5-b]pyridine-2-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 3H-Imidazo[4,5-b]pyridine-2-carboxylic acid
    • 1H-Imidazo[4,5-b]pyridine-2-carboxylic acid
    • BIQRPLMAKJWHIH-UHFFFAOYSA-N
    • 6832AC
    • AK104948
    • AB0187731
    • imidazo-[4,5-b]pyridine-2-carboxylic acid
    • BB 0261481
    • 1H-Imidazo[4,5-b]pyridine-2-carboxylic acid (9CI)
    • 3H-Imidazo[4,5-b]pyridine-2-carboxylicacid
    • DTXSID20626908
    • ALBB-016500
    • DB-088907
    • AKOS006292183
    • CS-0155700
    • MFCD05721719
    • SCHEMBL523396
    • 97640-15-8
    • SY084808
    • AS-65734
    • MDL: MFCD05721719
    • Inchi: 1S/C7H5N3O2/c11-7(12)6-9-4-2-1-3-8-5(4)10-6/h1-3H,(H,11,12)(H,8,9,10)
    • InChI Key: BIQRPLMAKJWHIH-UHFFFAOYSA-N
    • SMILES: O=C(C1NC2C(=NC=CC=2)N=1)O

Computed Properties

  • Exact Mass: 163.038176411g/mol
  • Monoisotopic Mass: 163.038176411g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 197
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 78.9
  • XLogP3: 0.6

3H-Imidazo[4,5-b]pyridine-2-carboxylic acid Security Information

  • HazardClass:IRRITANT

3H-Imidazo[4,5-b]pyridine-2-carboxylic acid Pricemore >>

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3H-Imidazo[4,5-b]pyridine-2-carboxylic acid Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Sodium carbonate ,  Permanganic acid (HMnO4), potassium salt (1:1) Solvents: Water ;  4 h, reflux; reflux → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  pH 2, rt
Reference
Preparation and formulation of N-quinuclidinyl-heteroaryls as nicotinic acetylcholinergic receptor modulators for the treatment of a variety of central nervous system disorders
, World Intellectual Property Organization, , ,

Production Method 2

Reaction Conditions
Reference
Preparation of 3-propenylcephem derivatives as antibacterial agents
, World Intellectual Property Organization, , ,

Production Method 3

Reaction Conditions
Reference
Synthesis and tuberculostatic activity of some derivatives of imidazo[4,5-b]pyridine-2-carboxylic acid
Bukowski, Ludwik, Polish Journal of Pharmacology and Pharmacy, 1984, 36(6), 683-8

3H-Imidazo[4,5-b]pyridine-2-carboxylic acid Raw materials

3H-Imidazo[4,5-b]pyridine-2-carboxylic acid Preparation Products

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