117680-13-4

Basic information

• Product Name: spermexatol
• Synonyms: spermexatol
• CAS NO: 117680-13-4
• Molecular Formula: C₂₆H₃₄N₄O₉
• Molecular Weight: 546.56956
• Mol File: 117680-13-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.38g/cm³
• Refractive Index: 1.628
• PKA: 8.20±0.35(Predicted)
• CAS DataBase Reference: spermexatol(CAS DataBase Reference)
• NIST Chemistry Reference: spermexatol(117680-13-4)
• EPA Substance Registry System: spermexatol(117680-13-4)

Safety Data

• Hazardous Substances Data: 117680-13-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C26H34N4O9/c1-29(39)21(33)11-12-22(34)30(16-6-14-28-26(38)18-8-5-10-20(32)24(18)36)15-3-2-13-27-25(37)17-7-4-9-19(31)23(17)35/h4-5,7-10,31-32,35-36,39H,2-3,6,11-16H2,1H3,(H,27,37)(H,28,38)

Upstream product

• 117680-06-5 N⁴-((p-Nitrobenzyl)succinoyl)-N¹,N⁸-bis(2,3-bis(benzyloxy)benzoyl)spermidine 
• 117680-09-8 N⁴-Succinoyl-N¹,N⁸-bis(2,3-bis(benzyloxy)benzoyl)spermidine 
• 117679-93-3 Succinimido ester of N-methyl-N-(benzyloxy)succinamic acid 
• 117679-85-3 4-((benzyloxy)(methyl)amino)-4-oxobutanoic acid 
• 74272-81-4 2,3-bis(benzyloxy)-N-(3-(4-(2,3-bis(benzyloxy)benzamido)butylamino)propyl)benzamide 
• 2169-27-9 Methyl 2,3-bis(benzyloxy)benzoate 
• 74272-78-9 2,3-dibenzyloxybenzoic acid 
• 303-38-8 2,3-Dihydroxybenzoic acid 
• 2411-83-8 methyl-2,3-dihydroxybenzoate 
• 117680-11-2 N⁴-(N-Methyl-N-(benzyloxy)succinamoyl)-N¹,N⁸-bis(2,3-bis(benzyloxy)benzoyl)spermidine 

Relevant articles and documents

Spermexatin and Spermexatol: New Synthetic Spermidine-Based Siderophore Analogues

Syntheses of hexanediamine-based dihydroxamate (Hexamate), spermidine-based trihydroxamate (Spermexatins), and spermidine-based mixed siderophore analogues (Spermexatols) are described.Key intermediates include the N-hydroxysuccinimide esters of various hydroxamic acids, e.g., malonohydroxamate, succinohydroxamate, and glutarohydroxamate.These intermediates were synthesized, characterized, and incorporated as the ligating chains on spermidine.Also, mixed iron chelating compounds (Spermexatols) with both catechol and hydroxamic acid side chains were synthesized.Thereagent carbobenzoxyimidazole was employed to distinguish between the primary and secondary amino groups of spermidine.The ability of these iron chelators to stimulate microbial growth is also described.