1006031-03-3

Basic information

• Product Name: methyl 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamino)-benzoylamino)-benzoate
• Synonyms: methyl 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamino)-benzoylamino)-benzoate
• CAS NO: 1006031-03-3
• Molecular Weight: 563.651
• Mol File: 1006031-03-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamino)-benzoylamino)-benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamino)-benzoylamino)-benzoate(1006031-03-3)
• EPA Substance Registry System: methyl 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamino)-benzoylamino)-benzoate(1006031-03-3)

Safety Data

• Hazardous Substances Data: 1006031-03-3(Hazardous Substances Data)

Upstream product

• 681465-85-0 4-amino-3-isopropoxybenzoic acid methyl ester 
• 379261-85-5 3-(isopropyloxy)-4-nitrobenzoic acid 
• 713-52-0 methyl 3-hydroxy-4-nitrobenzoate 
• 619-14-7 3-hydroxy-4-nitro-benzoic acid 
• 159783-41-2 methyl 3-isopropyloxy-4-nitrobenzoate 
• 1006030-92-7 methyl 3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamino)-benzoate 
• 1006030-83-6 methyl 3-isopropoxy-4-(3-isopropoxy-4-nitro-benzoylamino)-benzoate 
• 1006031-13-5 methyl 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-nitro-benzoylamino)-benzoylamino)-benzoate 

Downstream Products

• 1006031-06-6 C₄₁H₄₆N₄O₁₁ 
• 1190360-14-5 3-isopropoxy-4-(3-isopropoxy-4-(3-isopropoxy-4-amino-benzoylamido)-benzoylamido)-benzoic acid 
• 1006031-11-3 C₅₁H₅₇N₅O₁₃ 
• 1006031-09-9 C₄₁H₄₈N₄O₉ 

Relevant articles and documents

Design and synthesis of oligoamide-based double α-helix mimetics

An extensive series of bis-oligobenzamides and bis-oligopyridylamides have been efficiently prepared and studied by X-ray analysis and computational methods. A modular synthesis led to double α-helix mimics bearing between two and ten branched side-chains. The inter-helix angle and distance can be tuned by varying the length and rigidity of the spacer, thereby reproducing the recognition domains of a range of super-secondary structures.

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.