tert-butyl 2-[(1-methyl-1H-pyrrol-2-yl)methyl]-1H-indole-1-carboxylate CAS 1449331-55-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1449331-55-8
Molecular FormulaC19H22N2O2
Molecular Weight310.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-butyl 2-[(1-methyl-1H-pyrrol-2-yl)methyl]-1H-indole-1-carboxylate CAS 1449331-55-8 chemical structure

Description

As a certified reference material (CRM), tert-butyl 2-[(1-methyl-1H-pyrrol-2-yl)methyl]-1H-indole-1-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

tert-butyl 2-[(1-methyl-1H-pyrrol-2-yl)methyl]-1H-indole-1-carboxylate (CAS 1449331-55-8), molecular formula C19H22N2O2 and molecular weight 310.39 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, tert-butyl 2-[(1-methyl-1H-pyrrol-2-yl)methyl]-1H-indole-1-carboxylate (C19H22N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 310.39 g/mol, it falls into the moderately-high-molecular-weight range. 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.

Physical & Chemical Properties

Molecular FormulaC19H22N2O2
Molecular Weight310.39 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 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Nitrogen Atoms2

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