Methyl 5-amino-3-chloro-4-methylthiophene-2-carboxylate CAS 778611-10-2

Purity 97%+In StockPharmaceutical Standards
CAS No.778611-10-2
Molecular FormulaC7H8ClNO2S
Molecular Weight205.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 5-amino-3-chloro-4-methylthiophene-2-carboxylate CAS 778611-10-2 chemical structure

Description

CATO supplies Methyl 5-amino-3-chloro-4-methylthiophene-2-carboxylate (CAS 778611-10-2), a certified reference material (molecular formula C7H8ClNO2S, MW 205.66 g/mol) for analytical method development and quality control.

The molecular framework of Methyl 5-amino-3-chloro-4-methylthiophene-2-carboxylate (C7H8ClNO2S) is characterized by an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 Methyl 5-amino-3-chloro-4-methylthiophene-2-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.

Physical & Chemical Properties

Molecular FormulaC7H8ClNO2S
Molecular Weight205.66 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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