3-((5-Bromopyrimidin-2-yl)amino)tetrahydrothiophene 1-oxide CAS 1384672-89-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1384672-89-2
Molecular FormulaC8H10BrN3OS
Molecular Weight276.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((5-Bromopyrimidin-2-yl)amino)tetrahydrothiophene 1-oxide CAS 1384672-89-2 chemical structure

Description

Structurally, 3-((5-Bromopyrimidin-2-yl)amino)tetrahydrothiophene 1-oxide (C8H10BrN3OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 276.15 g/mol, it falls into the medium-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

3-((5-Bromopyrimidin-2-yl)amino)tetrahydrothiophene 1-oxide (CAS 1384672-89-2) is a high-purity analytical reference standard with the molecular formula C8H10BrN3OS and a molecular weight of 276.15 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 3-((5-Bromopyrimidin-2-yl)amino)tetrahydrothiophene 1-oxide 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 FormulaC8H10BrN3OS
Molecular Weight276.15 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentBr-containing
Nitrogen Atoms3
Sulfur Atoms1

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