1-(4-Fluorophenyl)-3-methyl-4,5,6,7-tetrahydro-1h-pyrazolo[4,3-b]pyridine CAS 1383735-43-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1383735-43-0
Molecular FormulaC13H14FN3
Molecular Weight231.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Fluorophenyl)-3-methyl-4,5,6,7-tetrahydro-1h-pyrazolo[4,3-b]pyridine CAS 1383735-43-0 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

1-(4-Fluorophenyl)-3-methyl-4,5,6,7-tetrahydro-1h-pyrazolo[4,3-b]pyridine (CAS 1383735-43-0), molecular formula C13H14FN3 and molecular weight 231.27 g/mol, is a CATO reference standard with documented purity and traceability.

1-(4-Fluorophenyl)-3-methyl-4,5,6,7-tetrahydro-1h-pyrazolo[4,3-b]pyridine (C13H14FN3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 1-(4-Fluorophenyl)-3-methyl-4,5,6,7-tetrahydro-1h-pyrazolo[4,3-b]pyridine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC13H14FN3
Molecular Weight231.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms3

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