Methyl (E)-2-amino-5-(1-cyanoprop-1-en-2-yl)-4-methylthiophene-3-carboxylate CAS 4815-42-3

Purity 97%+In StockPharmaceutical Standards
CAS No.4815-42-3
Molecular FormulaC11H12N2O2S
Molecular Weight236.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (E)-2-amino-5-(1-cyanoprop-1-en-2-yl)-4-methylthiophene-3-carboxylate CAS 4815-42-3 chemical structure

Description

Methyl (E)-2-amino-5-(1-cyanoprop-1-en-2-yl)-4-methylthiophene-3-carboxylate (CAS 4815-42-3), molecular formula C11H12N2O2S and molecular weight 236.29 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C11H12N2O2S, Methyl (E)-2-amino-5-(1-cyanoprop-1-en-2-yl)-4-methylthiophene-3-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 236.29 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 (E)-2-amino-5-(1-cyanoprop-1-en-2-yl)-4-methylthiophene-3-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 FormulaC11H12N2O2S
Molecular Weight236.29 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
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms2
Sulfur Atoms1

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