147779-39-3

Upstream product

• 104-94-9 4-methoxy-aniline 
• 98-88-4 benzoyl chloride 
• 6705-03-9 2-Amino-5-methoxybenzoic acid 
• 102-50-1 2-methyl-4-methoxyaniline 
• 861791-59-5 2-benzoylamino-5-methoxy-4-nitro-benzoic acid 
• 5367-32-8 5-methoxy-2-nitrotoluene 
• 2581-34-2 3-methyl-4-nitrophenol 
• 70-11-1 α-bromoacetophenone 
• 57183-50-3 6-methoxy-2-phenyl-1H-quinolin-4-one 
• 861299-78-7 4-amino-2-benzoylamino-5-methoxy-benzoic acid 
• 61495-08-7 N-(4-methoxy-2-methylphenyl)benzamide 
• 5883-96-5 5-methoxy-2-phenylindole 

Downstream Products

• 35673-25-7 6-methoxy-2-phenyl-4H-benzo[d][1,3]oxazin-4-one 

Relevant academic research and scientific papers

From Methaqualone and Beyond: Structure - Activity Relationship of 6-, 7-, and 8-Substituted 2,3-Diphenyl-quinazolin-4(3H)-ones and in Silico Prediction of Putative Binding Modes of Quinazolin-4(3H)-ones as Positive Allosteric Modulators of GABAA

Methaqualone (2-methyl-3-(o-tolyl)-quinazolin-4(3H)-one, MTQ) is a moderately potent positive allosteric modulator (PAM) of GABAA receptors (GABAARs). In a previous structure-activity relationship (SAR) study probing the importance of 2- and 3-substituent

Production of 3-Benzoyl-2,1-benzisoxazoles, 2-Phenyl-4H-3,1-benzoxazin-4-ones, and Novel Quinolinone Derivatives from 2-Phenylquinolin-4(1H)-ones and Sodium Dichloroisocyanurate

A simple synthesis of certain 3-benzoyl-2,1-benzisoxazoles 6 is accomplished via treatment of the corresponding 2-phenylquinolin-4(1H)-one 1 with sodium dichloroisocyanurate 2 in methanolic aq. alkali; the isomeric 2-phenyl-4H-3,1-benzoxazin-4-one 7 is al