tert-Butyl (1r,4r)-4-((Z)-2-iodovinyl)-cyclohexylcarbamate CAS 1452485-43-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1452485-43-6
Molecular FormulaC13H22INO2
Molecular Weight351.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (1r,4r)-4-((Z)-2-iodovinyl)-cyclohexylcarbamate CAS 1452485-43-6 chemical structure

Description

tert-Butyl (1r,4r)-4-((Z)-2-iodovinyl)-cyclohexylcarbamate (CAS 1452485-43-6), molecular formula C13H22INO2 and molecular weight 351.22 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, tert-Butyl (1r,4r)-4-((Z)-2-iodovinyl)-cyclohexylcarbamate is typically white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 351.22 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

As a certified reference material (CRM), tert-Butyl (1r,4r)-4-((Z)-2-iodovinyl)-cyclohexylcarbamate 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 FormulaC13H22INO2
Molecular Weight351.22 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.)1992
Halogen ContentI-containing
Nitrogen Atoms1

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