N-Boc-2-bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine CAS 949922-62-7

Purity 97%+In StockPharmaceutical Standards
CAS No.949922-62-7
Molecular FormulaC12H16BrNO2S
Molecular Weight318.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Boc-2-bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine CAS 949922-62-7 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.

CATO supplies N-Boc-2-bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine (CAS 949922-62-7), a certified reference material (molecular formula C12H16BrNO2S, MW 318.23 g/mol) for analytical method development and quality control.

N-Boc-2-bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine (C12H16BrNO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures N-Boc-2-bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine 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 FormulaC12H16BrNO2S
Molecular Weight318.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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