3-[(1,2,3,4-tetrahydroisoquinolin-2-yl)methyl]phenol CAS 414881-77-9

Purity 97%+In StockPharmaceutical Standards
CAS No.414881-77-9
Molecular FormulaC16H17NO
Molecular Weight239.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(1,2,3,4-tetrahydroisoquinolin-2-yl)methyl]phenol CAS 414881-77-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 239.31 g/mol gives 3-[(1,2,3,4-tetrahydroisoquinolin-2-yl)methyl]phenol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3-[(1,2,3,4-tetrahydroisoquinolin-2-yl)methyl]phenol (CAS 414881-77-9), a certified reference material (molecular formula C16H17NO, MW 239.31 g/mol) for analytical method development and quality control.

Structurally, 3-[(1,2,3,4-tetrahydroisoquinolin-2-yl)methyl]phenol (C16H17NO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 239.31 g/mol, it falls into the medium-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.

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), 3-[(1,2,3,4-tetrahydroisoquinolin-2-yl)methyl]phenol 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 FormulaC16H17NO
Molecular Weight239.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms1

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