Tert-butyl 3-formyl-7-methyl-1H-indole-1-carboxylate CAS 914348-96-2

Purity 97%+In StockPharmaceutical Standards
CAS No.914348-96-2
Molecular FormulaC15H17NO3
Molecular Weight259.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 3-formyl-7-methyl-1H-indole-1-carboxylate CAS 914348-96-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 259.30 g/mol gives Tert-butyl 3-formyl-7-methyl-1H-indole-1-carboxylate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Tert-butyl 3-formyl-7-methyl-1H-indole-1-carboxylate (CAS 914348-96-2), a certified reference material (molecular formula C15H17NO3, MW 259.30 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, Tert-butyl 3-formyl-7-methyl-1H-indole-1-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 259.30 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 Tert-butyl 3-formyl-7-methyl-1H-indole-1-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 FormulaC15H17NO3
Molecular Weight259.30 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 chloroform, dichloromethane, ethyl acetate, DMSO
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.)1987
Nitrogen Atoms1

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