80389-40-8

Basic information

• Product Name: Benzoic acid, 2-amino-3-methoxy-5-methyl-
• CAS NO: 80389-40-8
• Molecular Formula: C9H11NO3
• Molecular Weight: 181.191
• Mol File: 80389-40-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-amino-3-methoxy-5-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-amino-3-methoxy-5-methyl-(80389-40-8)
• EPA Substance Registry System: Benzoic acid, 2-amino-3-methoxy-5-methyl-(80389-40-8)

Safety Data

• Hazardous Substances Data: 80389-40-8(Hazardous Substances Data)

Upstream product

• 98922-98-6 2'-hydroxy-2,2,4'-trimethylpropionanilide 
• 74510-40-0 N-(2-methoxy-4-methylphenyl)pivalamide 
• 39538-68-6 2-methoxy-4-methylaniline 
• 106-49-0 p-toluidine 
• 147699-88-5 N-acetyl-2-bromo-6-methoxy p-toluidine 
• 147699-87-4 2-bromo-6-methoxy-p-toluidine 
• 6968-24-7 2,6-Dibromo-4-methylaniline 
• 80389-39-5 N-<2-(1-hydroxy-2-methylpropyl)>-2,3-dimethoxy-5-methylbenzamide 
• 76959-16-5 4,5-dihydro-2-(2,3-dimethoxy-5-methylphenyl)-4,4-dimethyloxazole 
• 5653-56-5 2,3-dimethoxy-5-methylbenzoic acid 
• 147699-89-6 N-acetyl-3-methoxy-5-methyl anthranilic acid 
• 76959-17-6 4,4-dimethyl-2-(2-amino-3-methoxy-5-methylphenyl)-oxazoline 
• 124-38-9 carbon dioxide 
• 74510-41-1 2-(2,2-Dimethyl-propionylamino)-3-methoxy-5-methyl-benzoic acid 

Downstream Products

• 76191-51-0 8-hydroxy-1-methoxy-3-methyl-5H-benzonaphtho<2,3-b>pyran-5,7,12-trione 
• 74510-47-7 {2-Chloro-3-methoxy-5-[2-methyl-2-(1-methyl-1H-imidazol-2-ylsulfanyl)-but-3-enyl]-phenyl}-methyl-carbamic acid methyl ester 
• 74510-51-3 {(E)-4-[4-Chloro-3-methoxy-5-(methoxycarbonyl-methyl-amino)-phenyl]-3-methyl-but-2-enyl}-phosphonic acid diethyl ester 
• 74510-50-2 [2-Chloro-5-((E)-4-iodo-2-methyl-but-2-enyl)-3-methoxy-phenyl]-methyl-carbamic acid methyl ester 
• 74510-46-6 (5-Bromomethyl-2-chloro-3-methoxy-phenyl)-methyl-carbamic acid methyl ester 
• 74510-45-5 (2-Chloro-3-methoxy-5-methyl-phenyl)-methyl-carbamic acid methyl ester 
• 74510-44-4 (2-Chloro-3-methoxy-5-methyl-phenyl)-carbamic acid methyl ester 
• 74510-43-3 2-Chloro-3-methoxy-5-methyl-benzoic acid 
• 90605-50-8 [5-((E)-4-Bromo-2-methyl-but-2-enyl)-2-chloro-3-methoxy-phenyl]-methyl-carbamic acid methyl ester 
• 90605-47-3 [2-Chloro-5-((E)-4-hydroxy-2-methyl-but-2-enyl)-3-methoxy-phenyl]-methyl-carbamic acid methyl ester 
• 155722-67-1 3-bromo-2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone 
• 155722-63-7 3-bromo-2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyl-5,6,7,8-tetrahydrojuglone 
• 155722-68-2 2-(2-methoxycarbonyl-6-methoxy-4-methyl)phenyljuglone 
• 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.

Synthesis of The Gilvocarcin-M Aglycone

The synthesis of the aglycone of the antibiotic Gilvocarcin-M by a sequential Meerwein Diels-Alder route is reported.The D-ring of the aglycone is attached by a halogen atom directed Meerwein arylation reaction and the A-ring is attached by a halogen atom directed Diels-Alder reaction.In the key step the directing chlorine atom is removed by a new thiophenylation reduction sequence.

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