Methyl 2-bromo-4H-pyrrolo[2,3-d]thiazole-5-carboxylate CAS 1934708-90-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1934708-90-3
Molecular FormulaC7H5BrN2O2S
Molecular Weight261.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 2-bromo-4H-pyrrolo[2,3-d]thiazole-5-carboxylate CAS 1934708-90-3 chemical structure

Description

CATO manufactures Methyl 2-bromo-4H-pyrrolo[2,3-d]thiazole-5-carboxylate 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 Methyl 2-bromo-4H-pyrrolo[2,3-d]thiazole-5-carboxylate (CAS 1934708-90-3), a certified reference material (molecular formula C7H5BrN2O2S, MW 261.10 g/mol) for analytical method development and quality control.

Structurally, Methyl 2-bromo-4H-pyrrolo[2,3-d]thiazole-5-carboxylate (C7H5BrN2O2S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 261.10 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC7H5BrN2O2S
Molecular Weight261.10 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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; 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.)1996
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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