201535-45-7

Basic information

• Product Name: N-(6-Amino-1-aminomethyl-hexyl)-2,3-bis-benzyloxy-benzamide
• CAS NO: 201535-45-7
• Molecular Weight: 461.604
• Mol File: 201535-45-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(6-Amino-1-aminomethyl-hexyl)-2,3-bis-benzyloxy-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(6-Amino-1-aminomethyl-hexyl)-2,3-bis-benzyloxy-benzamide(201535-45-7)
• EPA Substance Registry System: N-(6-Amino-1-aminomethyl-hexyl)-2,3-bis-benzyloxy-benzamide(201535-45-7)

Safety Data

• Hazardous Substances Data: 201535-45-7(Hazardous Substances Data)

Upstream product

• 201535-39-9 2-(2,3-Bis-benzyloxy-benzoylamino)-heptanedioic acid dimethyl ester 
• 201535-41-3 2-(2,3-Bis-benzyloxy-benzoylamino)-heptanedioic acid diamide 
• 53931-78-5 2-Amino-heptanedioic acid dimethyl ester; hydrochloride 
• 627-76-9 alpha-aminopimelic acid 

Downstream Products

• 201535-47-9 1,2,7-tris-[(2,3-dibenzyloxybenzoyl)amino]heptane 

Relevant articles and documents

Myxochelins B, C, D, E and F: A new structural principle for powerful siderophores imitating nature

The synthesis of the natural siderophore myxochelin B (1s) and its enantiomer 1R is described. 1s and 1R served as precursors for the synthesis of new hexadentate siderophores, the myxochelins C (7S) and CR (7R), D (14S) and DR (14R), E (19S) and (RS)-F (26R,S), with 2,3-dihydroxybenzoate (DHB) ligands and the simple backbones of asymmetric 1,2,n-triamino-n-alkanes. For the myxochelins C, D, E and F n is 6 (from lysine), 5 (from omithin), 4 (from asparagine amide) and 7 [from (±)-2-aminopimelic acid], respectively. The additional amino functions in the starting compounds were provided by dehydration of the corresponding primary amides, and subsequent reduction of the nitriles by cobalt boride in methanol. All new siderophores supply bacteria with ferric ions with an efficiency which depends on their chain length and stereochemistry. They show significant activity against the cytomegalo virus.