93796-85-1

Basic information

• Product Name: Benzene, 5-bromo-1-methoxy-3-methyl-2-nitro-
• CAS NO: 93796-85-1
• Molecular Formula: C8H8BrNO3
• Molecular Weight: 246.06
• Mol File: 93796-85-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzene, 5-bromo-1-methoxy-3-methyl-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 5-bromo-1-methoxy-3-methyl-2-nitro-(93796-85-1)
• EPA Substance Registry System: Benzene, 5-bromo-1-methoxy-3-methyl-2-nitro-(93796-85-1)

Safety Data

• Hazardous Substances Data: 93796-85-1(Hazardous Substances Data)

Upstream product

• 108-39-4 3-methyl-phenol 
• 29578-83-4 3-bromo-5-methoxytoluene 
• 74204-00-5 3-bromo-5-methylphenol 
• 58169-99-6 2,3,4,6-tetrabromo-5-methyl-phenol 
• 93796-61-3 5-bromo-3-methyl-2-nitrophenol 
• 74-88-4 methyl iodide 

Downstream Products

• 5345-42-6 1-methoxy-3-methyl-2-nitro-benzene 
• 93796-67-9 methyl 2-methoxy-4-(3-methoxy-5-methyl-4-nitrophenoxy)-6-methylbenzoate 
• 93796-80-6 methyl 6-heptyl-5-iodo-4-(2-iodo-5-methoxy-3-methyl-4-nitrophenoxy)-2-methoxybenzoate 
• 93796-76-0 methyl 5-bromo-4-(2-bromo-5-methoxy-3-methyl-4-nitrophenoxy)-6-heptyl-2-methoxybenzoate 
• 93796-79-3 methyl 6-heptyl-5-iodo-2-methoxy-4-(3-methoxy-5-methyl-4-nitrophenoxy)benzoate 
• 93823-42-8 methyl 5-bromo-6-heptyl-2-methoxy-4-(3-methoxy-5-methyl-4-nitrophenoxy)benzoate 
• 93796-78-2 4-(4-Amino-2-bromo-5-methoxy-3-methyl-phenoxy)-3-bromo-2-heptyl-6-methoxy-benzoic acid methyl ester 
• 93796-77-1 methyl 5-bromo-4-(2-bromo-5-methoxy-3-methylphenoxy)-6-heptyl-2-methoxybenzoate 
• 93796-69-1 methyl 5-bromo-4-(2-bromo-5-methoxy-3-methyl-4-nitrophenoxy)-2-methoxy-6-methylbenzoate 
• 93796-68-0 methyl 5-bromo-2-methoxy-4-(3-methoxy-5-methyl-4-nitrophenoxy)-6-methylbenzoate 
• 93796-70-4 methyl 4-(4-amino-2-bromo-5-methoxy-3-methylphenoxy)-5-bromo-2-methoxy-6-methylbenzoate 
• 93796-71-5 methyl 5-bromo-4-(2-bromo-5-methoxy-3-methylphenoxy)-2-methoxy-6-methylbenzoate 
• 93796-75-9 methyl 6-heptyl-2-methoxy-4-(3-methoxy-5-methyl-4-nitrophenoxy)benzoate 

Relevant articles and documents

Naturally Occurring Dibenzofurans. Part 5. Synthesis of Melacarpic Acid

The total synthesis of the lichen dibenzofuran melacarpic acid (5) was achieved by intramolecular Ullman coupling of methyl 5-bromo-4-(2-bromo-5-methoxy-3-methylphenoxy)-6-heptyl-2-methoxybenzoate (48) or methyl 6-heptyl-5-iodo-4-(2-iodo-5-methoxy-3-methyl-4-nitrophenoxy)-2-methoxybenzoate (46) followed by appropriate transformations.