114482-48-3

Basic information

• Product Name: Benzamide, N-[3-[[[[2,3-bis(phenylmethoxy)benzoyl]amino]acetyl][4-[[2,3-bis(phenyl methoxy)benzoyl]amino]butyl]amino]propyl]-2,3-bis(phenylmethoxy)-
• CAS NO: 114482-48-3
• Molecular Formula: C72H70N4O10
• Molecular Weight: 1151.37
• Mol File: 114482-48-3.mol

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[3-[[[[2,3-bis(phenylmethoxy)benzoyl]amino]acetyl][4-[[2,3-bis(phenyl methoxy)benzoyl]amino]butyl]amino]propyl]-2,3-bis(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[3-[[[[2,3-bis(phenylmethoxy)benzoyl]amino]acetyl][4-[[2,3-bis(phenyl methoxy)benzoyl]amino]butyl]amino]propyl]-2,3-bis(phenylmethoxy)-(114482-48-3)
• EPA Substance Registry System: Benzamide, N-[3-[[[[2,3-bis(phenylmethoxy)benzoyl]amino]acetyl][4-[[2,3-bis(phenyl methoxy)benzoyl]amino]butyl]amino]propyl]-2,3-bis(phenylmethoxy)-(114482-48-3)

Safety Data

• Hazardous Substances Data: 114482-48-3(Hazardous Substances Data)

Upstream product

• 74272-80-3 N-(2,3-dibenzyloxybenzoyl)glycine 
• 74272-81-4 2,3-bis(benzyloxy)-N-(3-(4-(2,3-bis(benzyloxy)benzamido)butylamino)propyl)benzamide 
• 69146-58-3 2,3-bis(benzyloxy)benzoyl chloride 
• 945496-82-2 dibenzyloxybenzoyl glycine methyl ester 
• 2411-83-8 methyl-2,3-dihydroxybenzoate 
• 303-38-8 2,3-Dihydroxybenzoic acid 
• 81254-86-6 2,3-bis(benzyloxy)-1-((2-thioxothiazolidin-1-yl)carbonyl)benzene 
• 2169-27-9 Methyl 2,3-bis(benzyloxy)benzoate 
• 74272-78-9 2,3-dibenzyloxybenzoic acid 

Downstream Products

• 78217-89-7 N⁴--N¹,N⁸-bis(2,3-dihydroxybenzoyl)spermidine 

Relevant articles and documents

New synthetic probes of the iron transport system of Paracoccus denitrificans

A range of analogues of parabactin A 4 and agrobactin A 5 have been synthesised. All these compounds were able to chelate iron, and to promote the growth of iron-starved Paracoccus denitrificans to varying degrees. A degree of flexibility in the sideropho

Synthesis of Parabactin Analogues and Formation of Transition Metal Complexes of Parabactin and Related Compounds

Transition metal complexes of parabactin and its related synthetic spermidine catecholamides which lack the central o-hydroxyphenyloxazoline were studied by the potentiometric titration method, e.s.r. spectroscopy, and fast atom bombardment mass spectrometry (FAB-MS).Direct mass spectral sampling of the parabactin-Fe(III) complex in glycerol solution was first achieved by FAB-MS spectrometry, confirming that the composition of the parabactin-Fe(III) complex is (2-)*2Na(1+) and that the iron(III) ion binds with two catechols and an o-hydroxyphenyl-Δ2-oxazoline moiety in NaOH solution.The e.s.r. g value (4.5) of the parabactin-Fe(III) complex differed from those (4.3) of the 3:1 catechol-Fe(III) complex and other parabactin-related catecholamide-Fe(III) complexes.These results suggest that the structure of the parabactin-Fe(III) complex differs considerably from the regular octahedral structure of the 3:1 catechol-Fe(III) complex and may have a structure similar to the ferrimycobactin P-Fe(III) complex, in which the iron(III) lies exposed in a splayed V-shaped cleft and binds with five oxygens and one nitrogen in a very strained octahedron.