1'-(Tert-butoxycarbonyl)spiro[chromane-2,4'-piperidine]-4-carboxylic acid CAS 1009375-04-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1009375-04-5
Molecular FormulaC19H25NO5
Molecular Weight347.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1'-(Tert-butoxycarbonyl)spiro[chromane-2,4'-piperidine]-4-carboxylic acid CAS 1009375-04-5 chemical structure

Description

Structurally, 1'-(Tert-butoxycarbonyl)spiro[chromane-2,4'-piperidine]-4-carboxylic acid (C19H25NO5) contains a flavonoid 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 347.41 g/mol, it falls into the moderately-high-molecular-weight range. 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 supplies 1'-(Tert-butoxycarbonyl)spiro[chromane-2,4'-piperidine]-4-carboxylic acid (CAS 1009375-04-5), a certified reference material (molecular formula C19H25NO5, MW 347.41 g/mol) for analytical method development and quality control.

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

As a certified reference material (CRM), 1'-(Tert-butoxycarbonyl)spiro[chromane-2,4'-piperidine]-4-carboxylic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC19H25NO5
Molecular Weight347.41 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 methanol, acetonitrile, DMSO, water (slightly soluble)
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.)1988
Nitrogen Atoms1

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