3,4-Di(furan-2-yl)-1-(pyridin-2-yl)-5,6,7,8-tetrahydroisoquinoline CAS 692729-85-4

Purity 97%+In StockPharmaceutical Standards
CAS No.692729-85-4
Molecular FormulaC22H18N2O2
Molecular Weight342.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Di(furan-2-yl)-1-(pyridin-2-yl)-5,6,7,8-tetrahydroisoquinoline CAS 692729-85-4 chemical structure

Description

CATO manufactures 3,4-Di(furan-2-yl)-1-(pyridin-2-yl)-5,6,7,8-tetrahydroisoquinoline 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.

3,4-Di(furan-2-yl)-1-(pyridin-2-yl)-5,6,7,8-tetrahydroisoquinoline (CAS 692729-85-4), molecular formula C22H18N2O2 and molecular weight 342.39 g/mol, is a CATO reference standard with documented purity and traceability.

3,4-Di(furan-2-yl)-1-(pyridin-2-yl)-5,6,7,8-tetrahydroisoquinoline (C22H18N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

Physical & Chemical Properties

Molecular FormulaC22H18N2O2
Molecular Weight342.39 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 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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms2

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