881909-54-2

Basic information

• Product Name: Benzoic acid, 3-amino-5-bromo-4-(2-butenylamino)-, methyl ester
• CAS NO: 881909-54-2
• Molecular Formula: C12H15BrN2O2
• Molecular Weight: 299.167
• Mol File: 881909-54-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-amino-5-bromo-4-(2-butenylamino)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-amino-5-bromo-4-(2-butenylamino)-, methyl ester(881909-54-2)
• EPA Substance Registry System: Benzoic acid, 3-amino-5-bromo-4-(2-butenylamino)-, methyl ester(881909-54-2)

Safety Data

• Hazardous Substances Data: 881909-54-2(Hazardous Substances Data)

Upstream product

• 1588-83-6 4-amino-3-nitrobenzoic acid 
• 3987-92-6 methyl 4-amino-3-nitrobenzoate 
• 790254-17-0 methyl 3-bromo-4-[(E/Z)-but-2-enyl(trifluoroacetyl)amino]-5-nitrobenzoate 
• 790254-16-9 methyl 3-bromo-5-nitro-4-[(trifluoroacetyl)amino]benzoate 
• 105655-17-2 methyl 4-amino-3-bromo-5-nitrobenzoate 
• 881909-48-4 methyl 3-bromo-4-[(E/Z)-but-2-enylamino]-5-nitrobenzoate 

Downstream Products

• 790254-22-7 methyl 7-amino-3-ethyl-1H-indole-5-carboxylate 

Relevant articles and documents

Synthesis of indoles: Efficient functionalisation of the 7-position

Traditional strategies in indole chemistry do not allow high-yielding access to some substitution patterns such as 3,5,7-trisubstituted indoles. We report in this article the efficient synthesis of this type of indole. The Heck cyclisation strategy we use

Synthesis of 3,5,7-substituted indoles via heck cyclisation

Traditional strategies in indole chemistry do not allow high yielding access to some substitution patterns such as 3,5,7-trisubstituted indoles. We report in this article the efficient synthesis of this type of indole. The Heck cyclisation strategy we use