tert-Butyl spiro[chromene-2,4'-piperidine]-1'-carboxylate CAS 1207163-67-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1207163-67-4
Molecular FormulaC18H23NO3
Molecular Weight301.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl spiro[chromene-2,4'-piperidine]-1'-carboxylate CAS 1207163-67-4 chemical structure

Description

Structurally, tert-Butyl spiro[chromene-2,4'-piperidine]-1'-carboxylate (C18H23NO3) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 301.38 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies tert-Butyl spiro[chromene-2,4'-piperidine]-1'-carboxylate (CAS 1207163-67-4), a certified reference material (molecular formula C18H23NO3, MW 301.38 g/mol) for analytical method development and quality control.

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.

CATO manufactures tert-Butyl spiro[chromene-2,4'-piperidine]-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.

Physical & Chemical Properties

Molecular FormulaC18H23NO3
Molecular Weight301.38 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1

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