Tert-butyl 5'-hydroxy-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate CAS 2306264-40-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2306264-40-2
Molecular FormulaC15H19NO4
Molecular Weight277.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 5'-hydroxy-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate CAS 2306264-40-2 chemical structure

Description

CATO manufactures Tert-butyl 5'-hydroxy-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate 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.

Tert-butyl 5'-hydroxy-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate (CAS 2306264-40-2), molecular formula C15H19NO4 and molecular weight 277.32 g/mol, is a CATO reference standard with documented purity and traceability.

Tert-butyl 5'-hydroxy-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate (C15H19NO4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. 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.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC15H19NO4
Molecular Weight277.32 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, 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
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Nitrogen Atoms1

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