Benzyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate CAS 206867-89-2

Purity 97%+In StockPharmaceutical Standards
CAS No.206867-89-2
Molecular FormulaC15H20INO4
Molecular Weight405.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Benzyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate CAS 206867-89-2 chemical structure

Description

CATO manufactures Benzyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate 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.

CATO supplies Benzyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate (CAS 206867-89-2), a certified reference material (molecular formula C15H20INO4, MW 405.23 g/mol) for analytical method development and quality control.

Benzyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate (C15H20INO4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

Physical & Chemical Properties

Molecular FormulaC15H20INO4
Molecular Weight405.23 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2016
Halogen ContentI-containing
Nitrogen Atoms1

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