5-((tert-Butoxycarbonyl)amino)quinoline-2-carboxylic acid CAS 1023816-89-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1023816-89-8
Molecular FormulaC15H16N2O4
Molecular Weight288.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-((tert-Butoxycarbonyl)amino)quinoline-2-carboxylic acid CAS 1023816-89-8 chemical structure

Description

CATO supplies 5-((tert-Butoxycarbonyl)amino)quinoline-2-carboxylic acid (CAS 1023816-89-8), a certified reference material (molecular formula C15H16N2O4, MW 288.30 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, 5-((tert-Butoxycarbonyl)amino)quinoline-2-carboxylic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 288.30 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

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-((tert-Butoxycarbonyl)amino)quinoline-2-carboxylic 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 FormulaC15H16N2O4
Molecular Weight288.30 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

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