4-((4-(Tert-butyl)thiazol-2-yl)amino)-3-((furan-2-ylmethyl)amino)-4-oxobutanoic acid CAS 1023919-26-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1023919-26-7
Molecular FormulaC16H21N3O4S
Molecular Weight351.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-((4-(Tert-butyl)thiazol-2-yl)amino)-3-((furan-2-ylmethyl)amino)-4-oxobutanoic acid CAS 1023919-26-7 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.

CATO supplies 4-((4-(Tert-butyl)thiazol-2-yl)amino)-3-((furan-2-ylmethyl)amino)-4-oxobutanoic acid (CAS 1023919-26-7), a certified reference material (molecular formula C16H21N3O4S, MW 351.42 g/mol) for analytical method development and quality control.

The molecular framework of 4-((4-(Tert-butyl)thiazol-2-yl)amino)-3-((furan-2-ylmethyl)amino)-4-oxobutanoic acid (C16H21N3O4S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 4-((4-(Tert-butyl)thiazol-2-yl)amino)-3-((furan-2-ylmethyl)amino)-4-oxobutanoic 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 FormulaC16H21N3O4S
Molecular Weight351.42 g/mol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms3
Sulfur Atoms1

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