Methyl 4-amino-1-ethyl-1H-indole-6-carboxylate CAS 734532-90-2

Purity 97%+In StockPharmaceutical Standards
CAS No.734532-90-2
Molecular FormulaC12H14N2O2
Molecular Weight218.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-amino-1-ethyl-1H-indole-6-carboxylate CAS 734532-90-2 chemical structure

Description

Methyl 4-amino-1-ethyl-1H-indole-6-carboxylate (CAS 734532-90-2) is a high-purity analytical reference standard with the molecular formula C12H14N2O2 and a molecular weight of 218.25 g/mol.

The molecular framework of Methyl 4-amino-1-ethyl-1H-indole-6-carboxylate (C12H14N2O2) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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 4-amino-1-ethyl-1H-indole-6-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 FormulaC12H14N2O2
Molecular Weight218.25 g/mol
AppearanceOff-white to pale yellow crystalline powder
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.)1986
Nitrogen Atoms2

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