tert-Butyl (3-bromothieno[2,3-b]pyridin-2-yl)carbamate CAS 1042441-73-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1042441-73-5
Molecular FormulaC12H13BrN2O2S
Molecular Weight329.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (3-bromothieno[2,3-b]pyridin-2-yl)carbamate CAS 1042441-73-5 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

CATO supplies tert-Butyl (3-bromothieno[2,3-b]pyridin-2-yl)carbamate (CAS 1042441-73-5), a certified reference material (molecular formula C12H13BrN2O2S, MW 329.21 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H13BrN2O2S, tert-Butyl (3-bromothieno[2,3-b]pyridin-2-yl)carbamate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 329.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC12H13BrN2O2S
Molecular Weight329.21 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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