tert-Butyl 4-(2-bromophenoxy)piperidine-1-carboxylate CAS 444605-55-4

Purity 97%+In StockPharmaceutical Standards
CAS No.444605-55-4
Molecular FormulaC16H21BrNO3
Molecular Weight355.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 4-(2-bromophenoxy)piperidine-1-carboxylate CAS 444605-55-4 chemical structure

Description

tert-Butyl 4-(2-bromophenoxy)piperidine-1-carboxylate (CAS 444605-55-4), molecular formula C16H21BrNO3 and molecular weight 355.25 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, tert-Butyl 4-(2-bromophenoxy)piperidine-1-carboxylate (C16H21BrNO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.5, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 355.25 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 4-(2-bromophenoxy)piperidine-1-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 FormulaC16H21BrNO3
Molecular Weight355.25 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)6.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1

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