4-[6-(bromomethyl)-5h,6h-[1,2,4]triazolo[3,4-b][1,3]thiazol-3-yl]pyridine CAS 848207-44-3

Purity 97%+In StockPharmaceutical Standards
CAS No.848207-44-3
Molecular FormulaC10H9BrN4S
Molecular Weight297.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-[6-(bromomethyl)-5h,6h-[1,2,4]triazolo[3,4-b][1,3]thiazol-3-yl]pyridine CAS 848207-44-3 chemical structure

Description

Structurally, 4-[6-(bromomethyl)-5h,6h-[1,2,4]triazolo[3,4-b][1,3]thiazol-3-yl]pyridine (C10H9BrN4S) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 297.17 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

4-[6-(bromomethyl)-5h,6h-[1,2,4]triazolo[3,4-b][1,3]thiazol-3-yl]pyridine (CAS 848207-44-3) is a high-purity analytical reference standard with the molecular formula C10H9BrN4S and a molecular weight of 297.17 g/mol.

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

CATO manufactures 4-[6-(bromomethyl)-5h,6h-[1,2,4]triazolo[3,4-b][1,3]thiazol-3-yl]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 FormulaC10H9BrN4S
Molecular Weight297.17 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentBr-containing
Nitrogen Atoms4
Sulfur Atoms1

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