117358-63-1

Basic information

• Product Name: 7-{4-nitrophenyl}-10,10-dimethyl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one
• Synonyms: 7-{4-nitrophenyl}-10,10-dimethyl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one
• CAS NO: 117358-63-1
• Molecular Formula: C₂₅H₂₂N₂O₃
• Molecular Weight: 398.45378
• Mol File: 117358-63-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-{4-nitrophenyl}-10,10-dimethyl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-{4-nitrophenyl}-10,10-dimethyl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one(117358-63-1)
• EPA Substance Registry System: 7-{4-nitrophenyl}-10,10-dimethyl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one(117358-63-1)

Safety Data

• Hazardous Substances Data: 117358-63-1(Hazardous Substances Data)

Upstream product

• 134-32-7 1-amino-naphthalene 
• 555-16-8 4-nitrobenzaldehdye 
• 126-81-8 dimedone 

Downstream Products

• 117358-72-2 10,10-Dimethyl-7-(4-nitro-phenyl)-10,11-dihydro-9H-benzo[c]acridin-8-one 

Relevant articles and documents

L-Proline-catalysed one-pot synthesis of tetrahydrobenzo[c]acridin-8(7H)- ones at room temperature

Only 10 mol% of l-Proline in ethanol proved to be a very efficient catalyst for the one-pot synthesis of a wide variety of highly substituted tetrahydrobenzo[c]acridin-8(7H)-ones at room temperature. The key advantages of this process are high yields, cos

Ultrasound-promoted one-pot synthesis of 7-aryl-7,10,11,12- tetrahydrobenzo[c]acridin-8(9H)-one derivatives

A series of 7-aryl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives were synthesized via the three-component coupling from aromatic aldehydes, 1-naphthylamine, and 5,5-dimethylcyclohexane-1,3-dione catalyzed by stannous chloride dihydrate (SnCl

An efficient ultrasound-promoted method for the one-pot synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives

A new, efficient and general method for preparation of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives using ultrasound irradiation is reported. Under ultrasound, the reaction time is short, the yields are high and the reaction conditions are m

An efficient one-pot synthesis of polyhydrobenzoacridine-1-one derivatives under microwave irradiation without catalyst

A series of 3,3-dimethyl-9-substituted-1,2,3,4,9,10-hexahydrobenzo[c] acridine-1-ones and 3,3-dimethyl-9-substituted-1,2,3,4,9,10-hexahydrobenzo[a] acridine-1-ones were synthesized by the reaction of an aldehyde, α-naphthylamine or β-naphthylamine and dim

Synthesis and Spectra of 7-(o- and p-R-Phenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenzacridin-8-ones. Structure Correction of 1,2,3,4-Tetrahydro-2,2-dimethyl-5-aryl-6-aza-7,8-benzophenanthren-4-ones

It has been reported that dimedone added to α-arylidennaphthylamines in ethanol with formation of 1,4-addition products derivatives of 5-aryl-5,6,7,8,9,10-hexahydrobenzophenanthridin-7-ones, III, which are easily oxidized by chromic anhydride to the co