835889-78-6

Basic information

• Product Name: phosphoric acid 2-(4-{4-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-ethoxy]-benzoyl}-phenoxy)-ethyl ester di-tert-butyl ester
• Synonyms: phosphoric acid 2-(4-{4-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-ethoxy]-benzoyl}-phenoxy)-ethyl ester di-tert-butyl ester
• CAS NO: 835889-78-6
• Molecular Weight: 712.734
• Mol File: 835889-78-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: phosphoric acid 2-(4-{4-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-ethoxy]-benzoyl}-phenoxy)-ethyl ester di-tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: phosphoric acid 2-(4-{4-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-ethoxy]-benzoyl}-phenoxy)-ethyl ester di-tert-butyl ester(835889-78-6)
• EPA Substance Registry System: phosphoric acid 2-(4-{4-[2-(1-acetyl-5-methyl-7-nitro-2,3-dihydro-1H-indol-4-yloxy)-ethoxy]-benzoyl}-phenoxy)-ethyl ester di-tert-butyl ester(835889-78-6)

Safety Data

• Hazardous Substances Data: 835889-78-6(Hazardous Substances Data)

Upstream product

• 114031-67-3 [4-(4-hydroxybenzoyl)phenyl]-2,2-dimethyl propanoate 
• 112004-83-8 [4-[4-(2,2-dimethylpropanoyloxy)benzoyl]phenyl] 2,2-dimethylpropanoate 
• 770250-71-0 5-methylindolin-4-ol 
• 19499-82-2 5-(N,N-dimethylaminomethyl)indol-4-ol 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 19499-83-3 5-methylindol-4-ol 
• 835889-77-5 4-{2-[di(tert-butoxy)phosphoryloxy]ethoxy}-4'-(trimethylacetoxy)benzophenone 
• 835889-75-3 1-acetyl-4-[2-(tert-butyldimethylsilyloxy)ethoxy]-5-methyl-7-nitroindoline 
• 835889-74-2 1-acetyl-4-[2-(tert-butyldimethylsilyloxy)ethoxy]-5-methylindoline 
• 835889-76-4 4-(2-hydroxyethoxy)-4'-(trimethylacetoxy)benzophenone 
• 835889-73-1 1-acetyl-4-(2-hydroxyethoxy)-5-methylindoline 
• 770250-60-7 4-acetoxy-1-acetyl-5-methylindoline 
• 770250-79-8 1-acetyl-5-methylindolin-4-ol 
• 835889-70-8 1-acetyl-4-(2-hydroxyethoxy)-5-methyl-7-nitroindoline 

Relevant articles and documents

Optimised synthesis and photochemistry of antenna-sensitised 1-acyl-7-nitroindolines

Benzophenone antenna-sensitised 1-acyl-7-nitroindolines show a significantly enhanced extent of photochemical cleavage in aqueous solution over their non-sensitised analogues and release the carboxylate derived from their 1-acyl group. The present work in