78266-67-8

Basic information

• Product Name: Benzeneacetaldehyde, a-methyl-2-nitro-
• CAS NO: 78266-67-8
• Molecular Formula: C9H9NO3
• Molecular Weight: 179.175
• Mol File: 78266-67-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzeneacetaldehyde, a-methyl-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetaldehyde, a-methyl-2-nitro-(78266-67-8)
• EPA Substance Registry System: Benzeneacetaldehyde, a-methyl-2-nitro-(78266-67-8)

Safety Data

• Hazardous Substances Data: 78266-67-8(Hazardous Substances Data)

Upstream product

• 30096-07-2 methyl α-methyl-2-nitrobenzeneacetate 
• 64987-77-5 2-(2-nitrophenyl)propanol 
• 612-22-6 2-nitro(ethylbenzene) 
• 201230-82-2 carbon monoxide 
• 579-71-5 2-nitrostyrene 

Downstream Products

• 1296698-79-7 (S)-di-tert-butyl 1-(2-(2-nitrophenyl)-1-oxopropan-2-yl)hydrazine-1,2-dicarboxylate 
• 83-34-1 3-Methylindole 
• 603-76-9 1-methylindole 

Relevant articles and documents

Asymmetric approach towards the total synthesis of (+)-actinopyllic acid

This paper describes our efforts towards the asymmetric total synthesis of (+)-actinophyllic acid. Starting from the chiral oxazolidinone 9, an azocino [4,3-b]indolyl intermediate (5) possessing the A/B/C ring system and the C16 quaternary stereogenic center of actinophyllic acid has been synthesized. Key steps include a LHMDS-promoted condensation to establish the critical C2–C16 bond and a successive four-step transformation to assemble the eight-membered C-ring of the target molecule.

An Improved Preparation of 1-Hydroxyindole and the Synthesis of Some Related 3-Carboxylic Acids and 1-Methoxyindole-3-acetonitrile

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