155722-68-2

Basic information

• Product Name: 2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone
• CAS NO: 155722-68-2
• Molecular Weight: 352.343
• Mol File: 155722-68-2.mol

Chemical Properties

• CAS DataBase Reference: 2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone(155722-68-2)
• EPA Substance Registry System: 2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone(155722-68-2)

Safety Data

• Hazardous Substances Data: 155722-68-2(Hazardous Substances Data)

Upstream product

• 6968-24-7 2,6-Dibromo-4-methylaniline 
• 115475-74-6 methyl-3-methoxy-5-methyl anthranilate 
• 77199-82-7 7-bromo-5,8-dimethoxy-1-tetralone 
• 85755-06-2 7-bromo-5,8-dimethoxy-1,2,3,4-tetrahydro-1-naphthol 
• 80389-40-8 3-methoxy-5-methyl anthranilic acid 
• 106-49-0 p-toluidine 
• 147699-87-4 2-bromo-6-methoxy-p-toluidine 
• 147699-88-5 N-acetyl-2-bromo-6-methoxy p-toluidine 
• 147699-89-6 N-acetyl-3-methoxy-5-methyl anthranilic acid 
• 1026950-14-0 3-bromo-5,6,7,8-tetrahydrojuglone 
• 186581-53-3 diazomethane 
• 76191-52-1 WS-5995 B 
• 155722-67-1 3-bromo-2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone 

Downstream Products

• 76191-52-1 WS-5995 B 

Relevant articles and documents

A new convergent synthesis of WS-5995-B, an anticoccidial antibiotic from Streptomyces auranticolor

A new synthesis of WS-5995-B, an anticoccidial antibiotic isolated from Streptomyces auranticolor is reported via the coupling reaction between 3-bromo-5,6,7,8-tetrahydrojuglone, and 3-methoxy-5-methyl anthranilic acid. A simple method for the preparation of the anthranilate 7 starting from p-toluidine by shorter sequence is reported.

1,4-Naphtoquinone derivatives and their use in treating coccidiosis

1,4-naphthoquinone derivatives represented by the following general formula: STR1 (wherein R1 represents a hydrogen atom, a hydroxy group, a lower alkoxy group or an arylthio group, R2 represents a carboxy group, an esterified carbox