(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pyridin-2-ylmethyl)propanoic acid CAS 1260601-10-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1260601-10-2
Molecular FormulaC24H22N2O4
Molecular Weight402.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pyridin-2-ylmethyl)propanoic acid CAS 1260601-10-2 chemical structure

Description

(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pyridin-2-ylmethyl)propanoic acid (C24H22N2O4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pyridin-2-ylmethyl)propanoic acid (CAS 1260601-10-2), a certified reference material (molecular formula C24H22N2O4, MW 402.44 g/mol) for analytical method development and quality control.

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 (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pyridin-2-ylmethyl)propanoic acid 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 FormulaC24H22N2O4
Molecular Weight402.44 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2

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