Tert-butyl (1r)-5-benzyl-4-cyano-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate CAS 1214628-63-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1214628-63-3
Molecular FormulaC18H23N3O2
Molecular Weight313.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (1r)-5-benzyl-4-cyano-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate CAS 1214628-63-3 chemical structure

Description

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, Tert-butyl (1r)-5-benzyl-4-cyano-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 313.39 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Tert-butyl (1r)-5-benzyl-4-cyano-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (CAS 1214628-63-3), molecular formula C18H23N3O2 and molecular weight 313.39 g/mol, is a CATO reference standard with documented purity and traceability.

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 Tert-butyl (1r)-5-benzyl-4-cyano-2,5-diazabicyclo[2.2.1]heptane-2-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.

Physical & Chemical Properties

Molecular FormulaC18H23N3O2
Molecular Weight313.39 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms3

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