128225-08-1

Basic information

• Product Name: Benz[a]acridin-11(7H)-one, 8,9,10,12-tetrahydro-12-(4-methoxyphenyl)-9,9-dimethyl-
• CAS NO: 128225-08-1
• Molecular Formula: C26H25NO2
• Molecular Weight: 383.49
• Mol File: 128225-08-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benz[a]acridin-11(7H)-one, 8,9,10,12-tetrahydro-12-(4-methoxyphenyl)-9,9-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benz[a]acridin-11(7H)-one, 8,9,10,12-tetrahydro-12-(4-methoxyphenyl)-9,9-dimethyl-(128225-08-1)
• EPA Substance Registry System: Benz[a]acridin-11(7H)-one, 8,9,10,12-tetrahydro-12-(4-methoxyphenyl)-9,9-dimethyl-(128225-08-1)

Safety Data

• Hazardous Substances Data: 128225-08-1(Hazardous Substances Data)

Upstream product

• 3471-13-4 dimedone 
• 123-11-5 4-methoxy-benzaldehyde 
• 91-59-8 naphthalen-2-ylamine 
• 126-81-8 dimedone 
• 135-19-3 β-naphthol 
• 21255-16-3 N-[(4-methoxyphenyl)methylene]-2-naphthalenamine 

Downstream Products

• 128225-15-0 12-(4-Methoxy-phenyl)-9,9-dimethyl-9,10-dihydro-8H-benzo[a]acridin-11-one 

Relevant articles and documents

A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium

A clean and simple synthesis of benzo[c]acridine, benzo[a]acridine, pyrido[2,3-c]acridine and benzo[f]quinoline derivatives was accomplished in good to excellent yields via the reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium catalyzed by TEBA. The structures were characterized by 1H NMR, IR and elemental analysis, and confirmed by X-ray diffraction study.

The first example of glucose-containing Br?nsted acid synthesis and catalysis: Efficient synthesis of tetrahydrobenzo[α]xanthens and tetrahydrobenzo[α]acridines in water

Glucose sulfonic acid (GSA) was synthesized for the first time and used as an efficient catalyst for the preparation of tetrahydrobenzo[α]xanthens and tetrahydrobenzo[α]acridines via the reaction of aromatic aldehydes, 2-naphthol (or β-naphthylamine), and

A clean synthesis of polyhydroacridine and indenoquinoline derivatives catalyzed by triethylbenzylammonium chloride in aqueous media

An efficient and convenient synthesis of benzo[a]acridines and indeno[1,2-b]benzo[f]quinolines was achieved in high yields by the reaction of N-arylidenenaphthalen-2-amine with 1,3-dicarbonyl compounds catalyzed with triethylbenzylammmonium chloride (TEBA