1H-indol-3-yl 2-{[(tert-butoxy)carbonyl]aMino}acetate

1H-indol-3-yl 2-{[(tert-butoxy)carbonyl]aMino}acetate - Names and Identifiers

Name	[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid
Synonyms	N-Boc-(3-Indole)glycine N-BOC-2-(INDOLE-3-YL)-DL-GLYCINE 1H-indol-3-yl 2-{[(tert-butoxy)carbonyl]aMino}acetate [(tert-Butoxycarbonyl)amino](1H-indol-3-yl)acetic acid [(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid [(tert-Butoxycarbonyl)amino]-(1H-indol-3-yl)acetic acid 1H-Indole-3-acetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]- alpha-[[(1,1-Dimethylethoxy)carbonyl]amino]-1H-indole-3-acetic acid 1H-Indole-3-acetic acid, alpha-[[(1,1-dimethylethoxy)carbonyl]amino]-
CAS	58237-94-8
InChI	InChI=1/C15H18N2O4/c1-15(2,3)21-14(20)17-12(13(18)19)10-8-16-11-7-5-4-6-9(10)11/h4-8,12,16H,1-3H3,(H,17,20)(H,18,19)

1H-indol-3-yl 2-{[(tert-butoxy)carbonyl]aMino}acetate - Physico-chemical Properties

Molecular Formula	C15H18N2O4
Molar Mass	290.31
Density	1.290±0.06 g/cm3(Predicted)
Boling Point	520.5±45.0 °C(Predicted)
Flash Point	268.6°C
Vapor Presure	1.17E-11mmHg at 25°C
pKa	3.70±0.30(Predicted)
Storage Condition	2-8°C
Refractive Index	1.611

1H-indol-3-yl 2-{[(tert-butoxy)carbonyl]aMino}acetate - Introduction

[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid, chemical formula C14H17NO4, is an organic compound. It is a glycine derivative by attachment of the 3-indole group at the N-protecting group (Boc) amino group.

[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid is a white crystalline solid, soluble in organic solvents such as dimethyl sulfoxide and methylene chloride. It is stable at normal temperature, but may decompose under high temperature and strong acid conditions.

[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid has a wide range of applications in different fields. It is commonly used in organic synthesis as a carrier molecule for the synthesis of other indole group compounds. In addition, it can also be used as an intermediate for the synthesis of drug molecules, such as anti-cancer drugs.

[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid is usually synthesized by first synthesizing 3-indoleacetic acid and then reacting with N-protecting group methyl carbonate to produce [(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid.

Regarding safety information,[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid is relatively safe for humans and the environment under normal operating conditions. However, like most organic compounds, it may have an irritating effect on the respiratory system, skin and eyes, so it is necessary to take appropriate protective measures when used. During use and storage, care should be taken to avoid contact with oxidants and strong acids, and avoid high temperatures and fire sources. In the event of an accident, appropriate first aid measures should be taken immediately, such as flushing the affected area with plenty of water and seeking medical attention immediately. It is best to look for more detailed safety information in the Safety Data Sheet.

Last Update：2024-04-09 21:32:42