Ethyl 4-aminospiro[cyclohex[3]ene-1,9'-fluorene]-3-carboxylate CAS 6629-89-6

Purity 97%+In StockPharmaceutical Standards
CAS No.6629-89-6
Molecular FormulaC16H16N2O5S
Molecular Weight348.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 4-aminospiro[cyclohex[3]ene-1,9'-fluorene]-3-carboxylate CAS 6629-89-6 chemical structure

Description

CATO manufactures Ethyl 4-aminospiro[cyclohex[3]ene-1,9'-fluorene]-3-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.

CATO supplies Ethyl 4-aminospiro[cyclohex[3]ene-1,9'-fluorene]-3-carboxylate (CAS 6629-89-6), a certified reference material (molecular formula C16H16N2O5S, MW 348.37 g/mol) for analytical method development and quality control.

The molecular framework of Ethyl 4-aminospiro[cyclohex[3]ene-1,9'-fluorene]-3-carboxylate (C16H16N2O5S) 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.

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 FormulaC16H16N2O5S
Molecular Weight348.37 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms2
Sulfur Atoms1

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