30464-85-8

Basic information

• Product Name: 6-Methoxy-1H-indole-2-methanol
• Synonyms: 6-Methoxy-1H-indole-2-methanol;(6-METHOXY-1H-INDOL-2-YL)METHANOL
• CAS NO: 30464-85-8
• Molecular Formula: C10H11NO2
• Molecular Weight: 177.19984
• Mol File: 30464-85-8.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Methoxy-1H-indole-2-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Methoxy-1H-indole-2-methanol(30464-85-8)
• EPA Substance Registry System: 6-Methoxy-1H-indole-2-methanol(30464-85-8)

Safety Data

• Hazardous Substances Data: 30464-85-8(Hazardous Substances Data)

Upstream product

• 98081-83-5 methyl 6-methoxy-1H-indole-2-carboxylate 
• 16732-73-3 6-Methoxyindole-2-carboxylic acid 
• 15050-04-1 6-methoxy-1H-indole-2-carboxylic acid ethyl ester 
• 62750-10-1 ethyl 2-((3-methoxyphenyl)amino)acetate 
• 536-90-3 m-Anisidine 

Downstream Products

• 30464-93-8 6-methoxy-1H-indole-2-carbaldehyde 
• 1402556-39-1 C₂₁H₂₁N₃O₇S 
• 1402556-40-4 C₂₃H₂₃N₃O₇S 
• 1402556-41-5 C₂₅H₂₇N₃O₈S 

Relevant articles and documents

Total synthesis of carbazole-1,4-quinone alkaloid koeniginequinones a and B based on a one-pot cyclocarbonylation procedure from 2-alkenyl-3-iodoindole

Total syntheses of koeniginequinones A and B, isolated from Murraya koenigii, were newly achieved by constructing of carbazole-1,4-quinone using a one-pot Pd-catalyzed cyclocarbonylation method with 2-(but-2-en-1-yl)-3-iodoindoles derived from known methyl 6-methoxyindole-2-carboxylate and methyl 5,6-dimethoxyindole-2-carboxylate, followed by desilylation, and an oxidation sequence.

AROMATIC RING DERIVATIVE AS IMMUNOREGULATION AND PREPARATION METHOD AND APPLICATION OF AROMATIC RING DERIVATIVE

Relating to a compound represented by formula (I) and a pharmaceutically acceptable salt of the compound, and an application of the compound as an S1P1 agonist.

Carbene-Catalyzed Enantioselective Aromatic N-Nucleophilic Addition of Heteroarenes to Ketones

The aromatic nitrogen atoms of heteroarylaldehydes are activated by carbene catalysts to react with ketone electrophiles. Multi-functionalized cyclic N,O-acetal products are afforded in good to excellent yields and optical purities. Our reaction involves the formation of an unprecedented aza-fulvene-type acylazolium intermediate. A broad range of N-heteroaromatic aldehydes and electron-deficient ketone substrates works effectively in this transformation. Several of the chiral N,O-acetal products afforded through this protocol exhibit excellent antibacterial activities against Ralstonia solanacearum (Rs) and are valuable in the development of novel agrichemicals for plant protection.