Description

tert-Butyl (2-(1H-indol-3-yl)ethyl)carbamate (CAS No. 103549-24-2) is a high-purity carbamate derivative widely used in organic synthesis and pharmaceutical research. This compound, with the molecular formula C₁₅H₂₀N₂O₂, features a tert-butyl carbamate group linked to a 2-(1H-indol-3-yl)ethyl moiety, making it a valuable intermediate for the synthesis of indole-containing bioactive molecules. Its IUPAC name is tert-butyl N-[2-(1H-indol-3-yl)ethyl]carbamate. This product is rigorously tested for quality, ensuring optimal performance in sensitive applications. Suitable for researchers and scientists, it is available in various packaging options to meet laboratory-scale and bulk requirements.

Properties

• CAS Number: 103549-24-2
• Complexity: 312
• IUPAC Name: tert-butyl N-[2-(1H-indol-3-yl)ethyl]carbamate
• InChI: InChI=1S/C15H20N2O2/c1-15(2,3)19-14(18)16-9-8-11-10-17-13-7-5-4-6-12(11)13/h4-7,10,17H,8-9H2,1-3H3,(H,16,18)
• InChI Key: UJUWQLXEMKUVGE-UHFFFAOYSA-N
• Exact Mass: 260.152477885
• Molecular Formula: C15H20N2O2
• Molecular Weight: 260.33
• SMILES: CC(C)(C)OC(=O)NCCC1=CNC2=CC=CC=C21
• Topological: 54.1
• Monoisotopic Mass: 260.152477885
• Synonyms: 103549-24-2, tert-Butyl (2-(1H-indol-3-yl)ethyl)carbamate, DTXSID60351126, tert-butyl [2-(1H-indol-3-yl)ethyl]carbamate, DTXCID60302193, boc-tryptamine, tert-butyl N-[2-(1H-indol-3-yl)ethyl]carbamate, tert-Butyl 2-(1H-indol-3-yl)ethylcarbamate, TERT-BUTOXYCARBONYL-TRYPTAMINE, MFCD00716928, ChemDiv2_004971, tert-butyl(2-(1H-Indol-3-yl)ethyl)carbamate, Oprea1_699359, SCHEMBL5745010, SCHEMBL8690644, N-(tert-Butoxycarbonyl)tryptamine, UJUWQLXEMKUVGE-UHFFFAOYSA-N, HMS1383B21, AB6707, STK755029, ZINC00063026, AKOS005615745, IDI1_003686, ST081778, DB-110147, CS-0314357, (tert-butoxy)-N-(2-indol-3-ylethyl)carboxamide, SR-01000515234, SR-01000515234-1

Application

tert-Butyl (2-(1H-indol-3-yl)ethyl)carbamate is commonly employed as a key intermediate in the synthesis of indole-based pharmaceuticals and agrochemicals. It serves as a protective group for amines in peptide and heterocyclic chemistry, enabling selective reactions. Researchers also utilize it in the development of serotonin receptor modulators and other neuroactive compounds due to its indole scaffold.

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