tert-Butyl(1R,4R)-5-iodo-2-azabicyclo[2.2.1]heptane-2-carboxylate CAS 2852760-69-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2852760-69-9
Molecular FormulaC11H18INO2
Molecular Weight323.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl(1R,4R)-5-iodo-2-azabicyclo[2.2.1]heptane-2-carboxylate CAS 2852760-69-9 chemical structure

Description

Structurally, tert-Butyl(1R,4R)-5-iodo-2-azabicyclo[2.2.1]heptane-2-carboxylate (C11H18INO2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 323.17 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

tert-Butyl(1R,4R)-5-iodo-2-azabicyclo[2.2.1]heptane-2-carboxylate (CAS 2852760-69-9), molecular formula C11H18INO2 and molecular weight 323.17 g/mol, is a CATO reference standard with documented purity and traceability.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures tert-Butyl(1R,4R)-5-iodo-2-azabicyclo[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 FormulaC11H18INO2
Molecular Weight323.17 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)2003
Halogen ContentI-containing
Nitrogen Atoms1

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