79465-86-4

Basic information

• Product Name: (2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate
• Synonyms: (2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate
• CAS NO: 79465-86-4
• Molecular Formula: C₁₆H₁₈N₂O₅
• Molecular Weight: 334.32392
• Mol File: 79465-86-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate(79465-86-4)
• EPA Substance Registry System: (2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate(79465-86-4)

Safety Data

• Hazardous Substances Data: 79465-86-4(Hazardous Substances Data)

Usage

General Description

"(2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate" is a chemical compound with a complex structure. It contains two methyl groups, an acetyl group, and two carboxylate groups, as well as a tetrahydro-pyrroloindole ring system. (2S)-diMethyl 8-acetyl-6-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indole-1,2(2H)-dicarboxylate is likely to have biological activity and potential pharmaceutical applications due to its unique structure. The presence of the acetyl and hydroxy groups suggests potential interactions with biological targets, and the tetrahydropyrroloindole core may confer specific pharmacological properties. Further research is needed to fully understand the potential uses and effects of this chemical.

Upstream product

• 66377-68-2 N_b-methoxycarbonyl-DL-tryptophan methyl ester 
• 108-24-7 acetic anhydride 
• 67811-38-5 DL-(2β,3aα,8aα)-1,2,3,3a,8,8a-hexahydro-1,2-dimethoxycarbonylpyrrolo<2,3-b>indole 
• 66377-68-2 N-(methoxycarbonyl)-L-tryptophan methyl ester 

Downstream Products

• 66377-68-2 N-(methoxycarbonyl)-L-tryptophan methyl ester 
• 107447-06-3 trans-1-isobutyl-7-methoxy-3-methoxycarbonyl-1,2,3,4-tetrahydro-β-carboline 
• 107447-05-2 (1S,3S)-methyl-1-isobutyl-7-methoxy-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylate 
• 107462-41-9 (1S,3S)-2-((S)-1-Benzyloxycarbonyl-pyrrolidine-2-carbonyl)-1-isobutyl-7-methoxy-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester 
• 107447-04-1 (S)-methyl 2-amino-3-(6-methoxy-1H-indol-3-yl)propanoate 
• 154-07-4 2-amino-3-(5-chloro-1H-indol-3-yl)propanoic acid 
• 6525-46-8 5-nitro-L-tryptophan 
• 6525-46-8 5-nitro-D-tryptophan 
• 93299-38-8 5-bromo-D-tryptophan methyl ester 
• 6548-09-0 5-bromo-L-tryptophan 
• 154-07-4 5-chloro-D-tryptophan 

Relevant articles and documents

CYCLIC TAUTOMERS OF TRYPTOPHANS AND TRYPTAMINES-4; SYNTHESIS OF CYCLIC TAUTOMERS OF TRYPTOPHANS AND TRYPTAMINES

Nb-Methoxycarbonyltryptophan methyl ester (DL- and L-13) was cyclized to the corresponding trans cyclic tautomer (14) in excellent yield in various acids such as 85percent phosphoric acid or trifluoroacetic acid.The cis cyclic tautomer (15) was formed as the less stable and kinetically controlled product and converted to the more stable trans isomer (14) under the reaction condition.The trans isomer (14) was reverted to 13 on treatment with 10percent sulfuric acid in methanol.Other tryptophan and tryptamine derivatives (6 and 19a) also cyclized to the corresponding cyclic tautomers in similar acidic media.