97444-12-7

Basic information

• Product Name: (2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid
• Synonyms: (2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid
• CAS NO: 97444-12-7
• Molecular Weight: 383.242
• Mol File: 97444-12-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid(97444-12-7)
• EPA Substance Registry System: (2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid(97444-12-7)

Safety Data

• Hazardous Substances Data: 97444-12-7(Hazardous Substances Data)

Usage

Description

(2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid is a chemical compound derived from propanoic acid, featuring an indole ring with a bromine substitution and a tert-butoxycarbonyl-protected amino group. Its unique structure and functional groups make it a valuable building block for pharmaceutical research and development.

Uses

Used in Pharmaceutical Research and Development:
(2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid is used as a building block for the synthesis of new drugs and therapeutic agents. Its unique structure and functional groups contribute to the creation of novel compounds with potential biological activity.
Used in Drug Synthesis:
(2S)-3-(6-bromo-1H-indol-3-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid is used as a key intermediate in the synthesis of pharmaceutical compounds, providing a versatile platform for the development of new drugs with improved efficacy and safety profiles.
Further investigation and experimentation are needed to fully understand the potential applications of this chemical in various industries.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 52448-17-6 (2S)-2-amino-3-(6-bromo-1H-indol-3-yl)propanoic acid 
• 85515-06-6 N^α-acetyl-6-bromo-D,L-tryptophan 
• 16732-65-3 6-bromo-indole-2-carboxylic acid(Ref_.7.) 
• 52415-29-9 6-bromo-1H-indole 
• 691-64-5 di-tert-butyl oxalate 
• 97444-11-6 (RS)-N-Acetyl-6-bromtryptophan-ethylester 
• 97444-10-5 3-(6-Brom-3-indolyl)-2-(hydroxyimino)propancarbonsaeure-ethylester 

Downstream Products

• 68857-44-3 Tetraacetylclionamid 
• 97444-13-8 6-Brom-N^α-(tert-butyloxycarbonyl)-N-<2-(4-nitrophenylseleno)-2-(3,4,5-triacetoxyphenyl)ethyl>tryptophanamid 
• 97444-01-4 6-Brom-N-<2-hydroxy-2-(3,4,5-triacetoxyphenyl)ethyl>-N^α-(tert-butyloxycarbonyl)tryptophanamid 
• 85515-02-2 O,O',O''-Triacetyl-N-(tert-butyloxycarbonyl)clionamid 
• 85515-01-1 6-Brom-N^α-(tert-butyloxycarbonyl)-N-<(3,4,5-triacetoxyphenyl)carbonylmethyl>tryptophanamid 
• 85515-04-4 (S)-6-Brom-N-(tert-butyloxycarbonyl)tryptophan-pentafluorphenylester 

Relevant articles and documents

Indole Alkaloids from the Sea Anemone Heteractis aurora and Homarine from Octopus cyanea

The two new indole alkaloids 2-amino-1,5-dihydro-5-(1H-indol-3-ylmethyl)-4H-imidazol-4-one (1), 2-amino-5-[(6-bromo-1H-indol-3-yl)methyl]-3,5-dihydro-3-methyl-4H-imidazol-4-one (2), and auramine (3) have been isolated from the sea anemone Heteractis auror

Amino acids and peptides, XLVIII. Total synthesis and biomimetic formation of clionamide derivatives

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