(R)-tert-Butyl (1-iodo-3-phenylpropan-2-yl)carbamate CAS 194096-74-7

Purity 97%+In StockPharmaceutical Standards
CAS No.194096-74-7
Molecular FormulaC14H20INO2
Molecular Weight361.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-tert-Butyl (1-iodo-3-phenylpropan-2-yl)carbamate CAS 194096-74-7 chemical structure

Description

CATO supplies (R)-tert-Butyl (1-iodo-3-phenylpropan-2-yl)carbamate (CAS 194096-74-7), a certified reference material (molecular formula C14H20INO2, MW 361.22 g/mol) for analytical method development and quality control.

Structurally, (R)-tert-Butyl (1-iodo-3-phenylpropan-2-yl)carbamate (C14H20INO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 361.22 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 (R)-tert-Butyl (1-iodo-3-phenylpropan-2-yl)carbamate 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 FormulaC14H20INO2
Molecular Weight361.22 g/mol
AppearanceOff-white 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2012
Halogen ContentI-containing
Nitrogen Atoms1

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