1-(6-Bromobenzo[d]thiazol-2-yl)azetidine-3-carboxylic acid CAS 1283109-52-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1283109-52-3
Molecular FormulaC11H9BrN2O2S
Molecular Weight313.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(6-Bromobenzo[d]thiazol-2-yl)azetidine-3-carboxylic acid CAS 1283109-52-3 chemical structure

Description

CATO manufactures 1-(6-Bromobenzo[d]thiazol-2-yl)azetidine-3-carboxylic acid 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.

CATO supplies 1-(6-Bromobenzo[d]thiazol-2-yl)azetidine-3-carboxylic acid (CAS 1283109-52-3), a certified reference material (molecular formula C11H9BrN2O2S, MW 313.17 g/mol) for analytical method development and quality control.

1-(6-Bromobenzo[d]thiazol-2-yl)azetidine-3-carboxylic acid (C11H9BrN2O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

Physical & Chemical Properties

Molecular FormulaC11H9BrN2O2S
Molecular Weight313.17 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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