41340-31-2

Usage

Uses

Used in Pharmaceutical Industry:
6-Methoxytryptophol is used as a bioactive compound for its potential therapeutic applications due to its antioxidant, anti-inflammatory, and immunomodulatory effects. It is being studied for its ability to regulate sleep and circadian rhythms, as well as for its potential in treating various neurological disorders.
Used in Nutraceutical Industry:
6-Methoxytryptophol is used as a dietary supplement for its health-promoting properties, including its antioxidant and anti-inflammatory activities, which can contribute to overall well-being and support the immune system.
Used in Research and Development:
6-Methoxytryptophol is used as a subject of study in scientific research for its potential role in understanding and developing treatments for sleep disorders, circadian rhythm regulation, and neurological conditions. Its diverse biological activities make it a valuable compound for exploring new therapeutic avenues in medicine.

Upstream product

• 68104-22-3 (6-methoxy-1H-indol-3-yl)(oxo)acetyl chloride 
• 68104-23-4 3-(2-Ethoxycarbonyl-1-oxoethyl)-6-methoxy indole 
• 408354-40-5 6-methoxy-1-methyl-α-oxo-1H-indole-3-acetic acid methyl ester 

Downstream Products

• 114383-33-4 5-methoxycarbonyl-2-[2-(6-methoxy-indol-3-yl)-ethyl]-isoquinolinium; bromide 
• 41340-09-4 (7-methoxy-1-propyl-1,3,4,9-tetrahydro-pyrano[3,4-b]indol-1-yl)-acetic acid 
• 68104-24-5 6-methoxy-tryptophyl bromide 
• 1534368-53-0 (3aR,8aS)-8-benzyl-6-methoxy-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indol-3a-ol 
• 1534368-72-3 C₁₇H₂₇NO₂Si 
• 1534368-73-4 C₂₄H₃₃NO₂Si 
• 1360548-54-4 trigonoliimine B 
• 1360548-53-3 3'-(2-(6-methoxy-1H-indol-3-yl)ethyl)-3'H-spiro[pyrrolidine-3,4'-quinazolin]-2-one 
• 1360548-52-2 3-(2-aminophenyl)-3-((2-(6-methoxy-1H-indol-3-yl)ethyl)amino)pyrrolidin-2-one 
• 1360548-51-1 3-((2-(6-methoxy-1H-indol-3-yl)ethyl)amino)-3-(2-nitrophenyl)pyrrolidin-2-one 
• 1360548-50-0 ethyl 4-azido-2-((2-(6-methoxy-1H-indol-3-yl)ethyl)amino)-2-(2-nitrophenyl)butanoate 
• 1360548-49-7 2-(6-methoxy-1H-indol-3-yl)acetaldehyde 
• 1195701-29-1 isoreserpinediol 
• 75276-05-0 C₄₂H₅₀N₂O₁₂ 

Relevant academic research and scientific papers

Dearomatization of tryptophols via a vanadium-catalyzed asymmetric epoxidation and ring-opening cascade

An enantioselective epoxidation of tryptophols followed by an intramolecular epoxide opening reaction was realized by chiral vanadium catalysts derived from C2 symmetric bis-hydroxamic acid (BHA) ligands. 3a-Hydroxyfuroindoline derivatives with up to 89% yield and 90% ee were obtained under mild reaction conditions.

5-Sulphanyl-4h-1,2,4-triazole derivatives and their use as medicine

The invention concerns novel 5-sulphanyl-4H-1,2,4-triazole derivatives of formula (1), wherein: R1, R2 and R3 represent variable groups and the methods for preparing them by liquid-phase parallel synthesis processes. Said product exhibit good affinity for certain sub-types of somatostatin receptors; they are particularly useful for treating pathological conditions or diseases wherein one (or more) somatostatin receptors is (are) involved. The invention also concerns pharmaceutical compositions containing said products and their use for preparing a medicine.

Convenient Synthesis of 6-Methoxyindole and 6-Methoxytryptophyl Bromide

A preparatively convenient synthesis of 6-methoxyindole (7) and 6-methoxytryptophylbromide (11) is presented starting with p-cresol (1).Regioselective nitration of p-cresol carbonate (2) followed by hydrolysis of the carbonate and methylation gives 4-methoxy-2-nitrotoluene (5) which is converted to 7 by esterification, reduction and bromination yields 6-methoxytryptophyl bromide (11).The overall yield of 7 and 11 from p-cresol is 43percent and 25percent respectively.