(1S,5S,6S)-tert-Butyl 5-bromo-8-oxo-7-oxa-3-azabicyclo[4.2.0]octane-3-carboxylate CAS 319911-72-3

Purity 97%+In StockPharmaceutical Standards
CAS No.319911-72-3
Molecular FormulaC11H16BrNO4
Molecular Weight306.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1S,5S,6S)-tert-Butyl 5-bromo-8-oxo-7-oxa-3-azabicyclo[4.2.0]octane-3-carboxylate CAS 319911-72-3 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

(1S,5S,6S)-tert-Butyl 5-bromo-8-oxo-7-oxa-3-azabicyclo[4.2.0]octane-3-carboxylate (CAS 319911-72-3), molecular formula C11H16BrNO4 and molecular weight 306.15 g/mol, is a CATO reference standard with documented purity and traceability.

(1S,5S,6S)-tert-Butyl 5-bromo-8-oxo-7-oxa-3-azabicyclo[4.2.0]octane-3-carboxylate (C11H16BrNO4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), (1S,5S,6S)-tert-Butyl 5-bromo-8-oxo-7-oxa-3-azabicyclo[4.2.0]octane-3-carboxylate 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 FormulaC11H16BrNO4
Molecular Weight306.15 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 methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1

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