1378949-53-1

Basic information

• Product Name: methyl 2-acetamido-4-(2-acetamido-4-(2-acetamido-5-methoxy-4-nitrobenzamido)-5-methoxybenzamido)-5-methoxybenzoate
• Synonyms: methyl 2-acetamido-4-(2-acetamido-4-(2-acetamido-5-methoxy-4-nitrobenzamido)-5-methoxybenzamido)-5-methoxybenzoate
• CAS NO: 1378949-53-1
• Molecular Weight: 680.628
• Mol File: 1378949-53-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-acetamido-4-(2-acetamido-4-(2-acetamido-5-methoxy-4-nitrobenzamido)-5-methoxybenzamido)-5-methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-acetamido-4-(2-acetamido-4-(2-acetamido-5-methoxy-4-nitrobenzamido)-5-methoxybenzamido)-5-methoxybenzoate(1378949-53-1)
• EPA Substance Registry System: methyl 2-acetamido-4-(2-acetamido-4-(2-acetamido-5-methoxy-4-nitrobenzamido)-5-methoxybenzamido)-5-methoxybenzoate(1378949-53-1)

Safety Data

• Hazardous Substances Data: 1378949-53-1(Hazardous Substances Data)

Upstream product

• 102-50-1 2-methyl-4-methoxyaniline 
• 196194-98-6 2-acetamido-5-methoxy-4-nitrobenzoic acid 
• 196194-97-5 N-(4-methoxy-2-methyl-5-nitrophenyl)acetamide 
• 31601-41-9 N-(4-methoxy-2-methylphenyl)acetamide 
• 1378949-50-8 methyl 2-acetamido-4-(2-acetamido-4-(2-amino-5-methoxy-4-nitrobenzamido)-5-methoxybenzamido)-5-methoxybenzoate hydrochloride 
• 75-36-5 acetyl chloride 
• 1378949-43-9 methyl 2-acetamido-4-(2-acetamido-5-methoxy-4-nitrobenzamido)-5-methoxybenzoate 
• 1378949-42-8 methyl 2-acetamido-4-(2-amino-5-methoxy-4-nitrobenzamido)-5-methoxybenzoate hydrochloride 
• 1378949-39-3 2-amino-5-methoxy-4-nitrobenzoic acid hydrochloride 
• 1378949-48-4 methyl 2-acetamido-4-(2-acetamido-4-amino-5-methoxybenzamido)-5-methoxybenzoate 

Relevant articles and documents

Double-sided α-helix mimetics

The design and synthesis of substituted bis- and tris-benzamides is reported in which the projection of side-chain residues on both sides of an α-helix is reproduced. The scaffold is conformationally constrained by a series of intramolecular hydrogen bonds, allowing for spatial and angular mimicry of the i, i+2, i+4 and i+6 side-chains in the case of the bis-benzamide, and may be extended to higher-order oligomers.