1006030-90-5

Basic information

• Product Name: methyl 3-isopropoxy-4-(3-(2-naphthylmethoxy)-4-nitro-benzoylamino)-benzoate
• Synonyms: methyl 3-isopropoxy-4-(3-(2-naphthylmethoxy)-4-nitro-benzoylamino)-benzoate
• CAS NO: 1006030-90-5
• Molecular Weight: 514.535
• Mol File: 1006030-90-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 3-isopropoxy-4-(3-(2-naphthylmethoxy)-4-nitro-benzoylamino)-benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-isopropoxy-4-(3-(2-naphthylmethoxy)-4-nitro-benzoylamino)-benzoate(1006030-90-5)
• EPA Substance Registry System: methyl 3-isopropoxy-4-(3-(2-naphthylmethoxy)-4-nitro-benzoylamino)-benzoate(1006030-90-5)

Safety Data

• Hazardous Substances Data: 1006030-90-5(Hazardous Substances Data)

Upstream product

• 1006030-80-3 3-((2-naphthylmethyl)oxy)-4-nitrobenzoic acid 
• 681465-85-0 4-amino-3-isopropoxybenzoic acid methyl ester 
• 1006030-78-9 methyl 3-((2-naphthylmethyl)oxy)-4-nitrobenzoate 
• 713-52-0 methyl 3-hydroxy-4-nitrobenzoate 
• 619-14-7 3-hydroxy-4-nitro-benzoic acid 

Downstream Products

• 1006030-96-1 methyl 3-isopropoxy-4-(3-(2-naphthylmethoxy)-4-amino-benzoylamino)-benzoate 

Relevant articles and documents

2-O-Alkylated para-benzamide α-helix mimetics: The role of scaffold curvature

The design and synthesis of a new 2-O-alklyated benzamide α-helix mimetic is described. Comparison with regioisomeric 3-O-alkylated benzamides permits a preliminary evaluation of the role that mimetic curvature has in determining molecular recognition properties.

Synthesis of functionalised aromatic oligamide rods

A current goal in synthetic chemistry is the design and synthesis of molecules that adopt well defined conformations - so called foldamers. In this manuscript we describe a modular approach for construction of rod shaped para-oligobenzamide molecules. Our approach permits regiospecific incorporation of side chains through a phenolic ether linkage on the scaffold; a feature that partly restricts the conformation of the rod through intramolecular hydrogen-bonding. The Royal Society of Chemistry 2008.