1160995-04-9

Basic information

• Product Name: tert-Butyl 3-(ethoxycarbonyl)-1H-indol-2-ylcarbaMate
• Synonyms: tert-Butyl 3-(ethoxycarbonyl)-1H-indol-2-ylcarbaMate;Ethyl 2-((tert-butoxycarbonyl)aMino)-1H-indole-3-carboxylate;2-[[(tert-Butoxyl)carbonyl]amino]-1H-indole-3-carboxylic acid ethyl ester;2-(BOC-AMINO)-1H-INDOLE-3-CARBOXYLIC ACID ETHYL ESTER
• CAS NO: 1160995-04-9
• Molecular Formula: C16H20N2O4
• Molecular Weight: 304.341
• Mol File: 1160995-04-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Density: 1.240
• Storage Temp.: 2-8°C
• CAS DataBase Reference: tert-Butyl 3-(ethoxycarbonyl)-1H-indol-2-ylcarbaMate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-Butyl 3-(ethoxycarbonyl)-1H-indol-2-ylcarbaMate(1160995-04-9)
• EPA Substance Registry System: tert-Butyl 3-(ethoxycarbonyl)-1H-indol-2-ylcarbaMate(1160995-04-9)

Safety Data

• Hazardous Substances Data: 1160995-04-9(Hazardous Substances Data)

Usage

General Description

Tert-Butyl 3-(ethoxycarbonyl)-1H-indol-2-ylcarbamate is a synthetic chemical compound that is commonly used as a building block in the production of pharmaceuticals and agrochemicals. It is a derivative of the indole compound, which is often associated with its use in the synthesis of anti-inflammatory and anti-cancer drugs. The tert-butyl group and the ethoxycarbonyl group in the compound provide stability and protection to the indole ring, making it a valuable intermediate for the production of various bioactive molecules. Additionally, the carbamate functional group in the compound makes it a versatile reactant in organic synthesis, allowing for the introduction of indole-based structures in organic molecules with specific biological activities.