1-tert-Butyl 3-methyl 1H-indole-1,3-dicarboxylate CAS 338760-26-2

Purity 97%+In StockPharmaceutical Standards
CAS No.338760-26-2
Molecular FormulaC15H17NO4
Molecular Weight275.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-tert-Butyl 3-methyl 1H-indole-1,3-dicarboxylate CAS 338760-26-2 chemical structure

Description

The molecular framework of 1-tert-Butyl 3-methyl 1H-indole-1,3-dicarboxylate (C15H17NO4) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 1-tert-Butyl 3-methyl 1H-indole-1,3-dicarboxylate (CAS 338760-26-2), a certified reference material (molecular formula C15H17NO4, MW 275.30 g/mol) for analytical method development and quality control.

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 1-tert-Butyl 3-methyl 1H-indole-1,3-dicarboxylate 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 FormulaC15H17NO4
Molecular Weight275.30 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms1

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