Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate CAS 1010120-60-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1010120-60-1
Molecular FormulaC9H10BrN3O2S
Molecular Weight304.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate CAS 1010120-60-1 chemical structure

Description

CATO manufactures Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate 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.

CATO supplies Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate (CAS 1010120-60-1), a certified reference material (molecular formula C9H10BrN3O2S, MW 304.16 g/mol) for analytical method development and quality control.

The molecular framework of Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate (C9H10BrN3O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC9H10BrN3O2S
Molecular Weight304.16 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms3
Sulfur Atoms1

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