2H-1-Benzopyran-7-ol, 3,4-dihydro-3-[(4-hydroxyphenyl)methyl]-, (3R)- CAS 1180504-64-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1180504-64-6
Molecular FormulaC16H16O3
Molecular Weight256.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2H-1-Benzopyran-7-ol, 3,4-dihydro-3-[(4-hydroxyphenyl)methyl]-, (3R)- CAS 1180504-64-6 chemical structure

Description

The molecular framework of 2H-1-Benzopyran-7-ol, 3,4-dihydro-3-[(4-hydroxyphenyl)methyl]-, (3R)- (C16H16O3) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

2H-1-Benzopyran-7-ol, 3,4-dihydro-3-[(4-hydroxyphenyl)methyl]-, (3R)- (CAS 1180504-64-6) is a high-purity analytical reference standard with the molecular formula C16H16O3 and a molecular weight of 256.30 g/mol.

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

CATO manufactures 2H-1-Benzopyran-7-ol, 3,4-dihydro-3-[(4-hydroxyphenyl)methyl]-, (3R)- 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 FormulaC16H16O3
Molecular Weight256.30 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989

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