1-(4-Bromothiophen-2-yl)-N-((5-chloro-1,2,3-thiadiazol-4-yl)methyl)-N-methylmethanamine CAS 1248916-87-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1248916-87-1
Molecular FormulaC9H9BrClN3S2
Molecular Weight338.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Bromothiophen-2-yl)-N-((5-chloro-1,2,3-thiadiazol-4-yl)methyl)-N-methylmethanamine CAS 1248916-87-1 chemical structure

Description

CATO manufactures 1-(4-Bromothiophen-2-yl)-N-((5-chloro-1,2,3-thiadiazol-4-yl)methyl)-N-methylmethanamine 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.

1-(4-Bromothiophen-2-yl)-N-((5-chloro-1,2,3-thiadiazol-4-yl)methyl)-N-methylmethanamine (CAS 1248916-87-1) is a high-purity analytical reference standard with the molecular formula C9H9BrClN3S2 and a molecular weight of 338.67 g/mol.

1-(4-Bromothiophen-2-yl)-N-((5-chloro-1,2,3-thiadiazol-4-yl)methyl)-N-methylmethanamine (C9H9BrClN3S2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, chlorine/bromine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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.

Physical & Chemical Properties

Molecular FormulaC9H9BrClN3S2
Molecular Weight338.67 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl/Br-containing
Nitrogen Atoms3
Sulfur Atoms2

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