tert-Butyl ((1r,4r)-4-(2-bromoethyl)cyclohexyl)carbamate CAS 1062468-06-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1062468-06-7
Molecular FormulaC13H24BrNO2
Molecular Weight306.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl ((1r,4r)-4-(2-bromoethyl)cyclohexyl)carbamate CAS 1062468-06-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including tert-Butyl ((1r,4r)-4-(2-bromoethyl)cyclohexyl)carbamate.

CATO supplies tert-Butyl ((1r,4r)-4-(2-bromoethyl)cyclohexyl)carbamate (CAS 1062468-06-7), a certified reference material (molecular formula C13H24BrNO2, MW 306.24 g/mol) for analytical method development and quality control.

Owing to an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, tert-Butyl ((1r,4r)-4-(2-bromoethyl)cyclohexyl)carbamate is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 306.24 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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,4r)-4-(2-bromoethyl)cyclohexyl)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 FormulaC13H24BrNO2
Molecular Weight306.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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.)1988
Halogen ContentBr-containing
Nitrogen Atoms1

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