ChemicalBook--->CAS DataBase List--->932702-11-9

932702-11-9

932702-11-9 Structure

932702-11-9 Structure
IdentificationBack Directory
[Name]

1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid
[CAS]

932702-11-9
[Synonyms]

1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid
1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid ISO 9001:2015 REACH
[Molecular Formula]

C7H5N3O2
[MDL Number]

MFCD11042720
[MOL File]

932702-11-9.mol
[Molecular Weight]

163.14
Chemical PropertiesBack Directory
[Boiling point ]

501.7±30.0 °C(Predicted)
[density ]

1.617
[storage temp. ]

Sealed in dry,2-8°C
[pka]

1.54±0.30(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315-H302
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
[HS Code ]

2933998090
Questions And AnswerBack Directory
[Application]

1H-pyrazolo[4,3-C]pyridine-3-carboxylic acid is an intermediate in organic synthesis and pharmaceutical research and development, and can be used in laboratory organic synthesis and chemical and pharmaceutical synthesis processes.
Spectrum DetailBack Directory
[Spectrum Detail]

1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid(932702-11-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Pyrazolo[4,3-c]pyridine-3-carboxamide, N,N-bis(1-methylethyl)-

932702-12-0

1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid

932702-11-9

1H-Pyrazolo[4,3-c]pyridine-3-carboxamide, N-(1-methylethyl)-

936923-48-7

The general procedure for the synthesis of 1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid and compound (CAS: 936923-48-7) using compound (CAS: 932702-12-0) as starting material was as follows: in a microwave reaction vessel, N,N-diisopropyl-1H-pyrazolo[4,3-c]pyridine-3-carboxamide (0.800 g. 0.00325 mol) was mixed with 10 M aqueous hydrogen chloride solution (3.00 mL). The mixture was heated at 120 °C for 10 min. Heating at high absorbance settings is required to avoid pressure buildup. After completion of the reaction, the reaction mixture was diluted with water and neutralized with 3 N sodium hydroxide solution. The resulting white precipitate was collected and analyzed and found to be a mixture of 1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid (47%) and monoisopropylamide (25%). The mixture could be used in subsequent steps without further purification.

[References]

[1] Patent: US2007/78147, 2007, A1. Location in patent: Page/Page column 69
[2] Patent: WO2007/56582, 2007, A1. Location in patent: Page/Page column 76
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