5-amino-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-2-one dihydrochloride CAS 1461704-92-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1461704-92-6
Molecular FormulaC11H11N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-amino-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-2-one dihydrochloride CAS 1461704-92-6 chemical structure

Description

Based on its molecular formula C11H11N3OHCl, 5-amino-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-2-one dihydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 237.69 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

5-amino-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-2-one dihydrochloride (CAS 1461704-92-6) is a high-purity analytical reference standard with the molecular formula C11H11N3OHCl and a molecular weight of 237.69 g/mol.

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

CATO manufactures 5-amino-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-2-one dihydrochloride 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 FormulaC11H11N3O 2*HCl
Molecular Weight237.69 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentCl-containing
Nitrogen Atoms3

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