545362-97-8

Usage

Molecular weight

374.23 g/mol This is the mass of one mole of the compound, based on the atomic weights of the elements that make it up.

Structure

1H-Indole-3-ethanol, 2-iodo-6,7-dimethoxy-, acetate (ester) This is a description of the arrangement of atoms in the molecule, including the types and positions of substituents.

Purity

Varies The purity of the compound can affect its properties and potential uses. The material provided does not specify the purity of the compound.

Stability

Varies The stability of the compound can affect its suitability for different applications. The material provided does not specify the stability of the compound.

Potential uses

Varies The material provided suggests that the compound may be useful in various chemical and pharmaceutical applications, but further research and testing would be necessary to fully explore its potential.

Upstream product

• 55149-84-3 2-nitroveratraldehyde 

Downstream Products

• 545362-99-0 (3S)-5-[3-(2-acetoxy-ethyl)-6,7-dimethoxy-1H-indol-2-yl]-3-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-dimethoxymethyl-pent-4-ynoic acid ethyl ester 
• 634911-89-0 (3S)-5-[3-(2-acetoxy-ethyl)-6,7-dimethoxy-1H-indol-2-yl]-3-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-[1,3]dioxolan-2-yl-pent-4-ynoic acid dimethylamide 
• 634911-90-3 (3'S)-3-(2-acetoxy-ethyl)-2-[6'-(tert-butyl-diphenyl-silanyloxy)-3'-dimethylcarbamoylmethyl-3'-[1,3]dioxolan-2''-yl-hexyl]-6,7-dimethoxy-indole-1-carboxylic acid tert-butyl ester 
• 634911-97-0 3-(2-Acetoxy-ethyl)-2-[(Z)-(S)-3-dimethoxymethyl-3-ethoxycarbonylmethyl-6-(2-nitro-benzenesulfonylamino)-hex-1-enyl]-6,7-dimethoxy-indole-1-carboxylic acid tert-butyl ester 
• 634912-20-2 (3S)-5-[3-(2-acetoxy-ethyl)-6,7-dimethoxy-1H-indol-2-yl]-3-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-[1,3]dioxolan-2-yl-pentanoic acid dimethylamide 
• 634911-92-5 (11R)-11-dimethylcarbamoylmethyl-11-[1,3]dioxolan-2-yl-1,2-dimethoxy-7-(2-nitrobenzenesulfonyl)-6,7,8,9,10,11,12,13-octahydro-5H-7,14-diazacycloundeca[a]indene-14-carboxylic acid tert-butyl ester 
• 634912-05-3 (11R)-11-dimethylcarbamoylmethyl-11-formyl-1,2-dimethoxy-7-(2-nitro-benzenesulfonyl)-6,7,8,9,10,11,12,13-octahydro-5H-7,14-diazacycloundeca[a]indene-14-carboxylic acid tert-butyl ester 
• 634911-98-1 ((3aR,10bS,12bS)-7,8-Dimethoxy-4-phenylsulfanyl-2,3,4,5,11,12-hexahydro-1H-6,12a-diaza-indeno[7,1-cd]fluoren-3a-yl)-acetic acid ethyl ester 
• 545363-30-2 (1'Z)-(3'S)-2-[6'-(tert-butyldiphenyl-silanyloxy)-3'-dimethoxymethyl-3'-ethoxycarbonylmethyl-hex-1'-enyl]-6,7-dimethoxy-3-[2-(2-nitro-benzenesulfonylamino)-ethyl]-indole-1-carboxylic acid tert-butyl ester 
• 545363-02-8 (1'Z)-(3'S)-3-(2-acetoxy-ethyl)-2-[6'-(tert-butyldiphenyl-silanyloxy)-3'-dimethoxymethyl-3'-ethoxycarbonylmethyl-hex-1'-enyl]-6,7-dimethoxyindole-1-carboxylic acid tert-butyl ester 
• 545363-28-8 (1'Z)-(3'S)-2-[6'-(tert-butyldiphenyl-silanyloxy)-3'-dimethoxymethyl-3'-ethoxycarbonylmethyl-hex-1'-enyl]-3-(2-hydroxy-ethyl)-6,7-dimethoxy-indole-1-carboxylic acid tert-butyl ester 
• 545363-04-0 (1'Z)-(3'S)-2-(3'-dimethoxymethyl-3'-ethoxycarbonylmethyl-6'-hydroxy-hex-1'-enyl)-6,7-dimethoxy-3-[2-(2-nitro-benzenesulfonylamino)-ethyl]-indole-1-carboxylic acid tert-butyl ester 
• 545363-06-2 (11S)-(12Z)-11-dimethoxymethyl-11-ethoxycarbonylmethyl-1,2-dimethoxy-7-(2-nitro-benzenesulfonyl)-6,7,8,9,10,11-hexahydro-5H-7,14-diaza-cycloundeca[a]indene-14-carboxylic acid tert-butyl ester 
• 545363-32-4 (11S)-(12Z)-11-ethoxycarbonylmethyl-11-formyl-1,2-dimethoxy-7-(2-nitro-benzenesulfonyl)-6,7,8,9,10,11-hexahydro-5H-7,14-diaza-cycloundeca[a]indene-14-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Enantioselective total synthesis of aspidophytine

(Matrix presented) An enantioselective total synthesis of aspidophytine is described. The indole fragment bearing a cis-alkene substituent was efficiently prepared through radical cyclization of a 2-alkenylphenylisocyanide followed by Sonogashira coupling of the generated 2-iodoindole derivative with a functionalized acetylene unit. After formation of the 11-membered cyclic amine, the aspidosperma skeleton and lactone ring were constructed to complete the total synthesis.