tert-butyl N-[(1R,3R)-3-(bromomethyl)cyclopentyl]carbamate CAS 2306254-13-5

Purity 97%+In StockPharmaceutical Standards
CAS No.2306254-13-5
Molecular FormulaC11H20BrNO2
Molecular Weight278.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-butyl N-[(1R,3R)-3-(bromomethyl)cyclopentyl]carbamate CAS 2306254-13-5 chemical structure

Description

Structurally, tert-butyl N-[(1R,3R)-3-(bromomethyl)cyclopentyl]carbamate (C11H20BrNO2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 2.0, corresponding to approximately 2 ring(s) or double-bond equivalent(s). With a molecular weight of 278.19 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies tert-butyl N-[(1R,3R)-3-(bromomethyl)cyclopentyl]carbamate (CAS 2306254-13-5), a certified reference material (molecular formula C11H20BrNO2, MW 278.19 g/mol) for analytical method development and quality control.

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 N-[(1R,3R)-3-(bromomethyl)cyclopentyl]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 FormulaC11H20BrNO2
Molecular Weight278.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1999
Halogen ContentBr-containing
Nitrogen Atoms1

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