91817-03-7

Basic information

• Product Name: 5,17-Dibenzyl-2,8,14,20-tetrabutyl-11,23-dichloro-2,5,8,10,12,14,17,20,22,24,25,26-dodecaaza-tricyclo[19.3.1.1^9,13]hexacosa-1⁽²⁵⁾,9,11,13⁽²⁶⁾,21,23-hexaene
• Synonyms: 5,17-Dibenzyl-2,8,14,20-tetrabutyl-11,23-dichloro-2,5,8,10,12,14,17,20,22,24,25,26-dodecaaza-tricyclo[19.3.1.1^9,13]hexacosa-1⁽²⁵⁾,9,11,13⁽²⁶⁾,21,23-hexaene
• CAS NO: 91817-03-7
• Molecular Weight: 833.994
• Mol File: 91817-03-7.mol

Chemical Properties

• CAS DataBase Reference: 5,17-Dibenzyl-2,8,14,20-tetrabutyl-11,23-dichloro-2,5,8,10,12,14,17,20,22,24,25,26-dodecaaza-tricyclo[19.3.1.1^9,13]hexacosa-1⁽²⁵⁾,9,11,13⁽²⁶⁾,21,23-hexaene(CAS DataBase Reference)
• NIST Chemistry Reference: 5,17-Dibenzyl-2,8,14,20-tetrabutyl-11,23-dichloro-2,5,8,10,12,14,17,20,22,24,25,26-dodecaaza-tricyclo[19.3.1.1^9,13]hexacosa-1⁽²⁵⁾,9,11,13⁽²⁶⁾,21,23-hexaene(91817-03-7)
• EPA Substance Registry System: 5,17-Dibenzyl-2,8,14,20-tetrabutyl-11,23-dichloro-2,5,8,10,12,14,17,20,22,24,25,26-dodecaaza-tricyclo[19.3.1.1^9,13]hexacosa-1⁽²⁵⁾,9,11,13⁽²⁶⁾,21,23-hexaene(91817-03-7)

Safety Data

• Hazardous Substances Data: 91817-03-7(Hazardous Substances Data)

Upstream product

• 91817-09-3 3-Benzyl-N,N'-dibutanoyl-3-aza-1,5-pentanediamine 
• 91817-11-7 N-Benzyl-N'-butyl-N-(2-butylamino-ethyl)-ethane-1,2-diamine 
• 91817-13-9 N-Benzyl-N'-butyl-N-{2-[butyl-(4,6-dichloro-[1,3,5]triazin-2-yl)-amino]-ethyl}-N'-(4,6-dichloro-[1,3,5]triazin-2-yl)-ethane-1,2-diamine 
• 23539-10-8 N¹-(2-aminoethyl)-N1-benzylethane-1,2-diamine 
• 23538-88-7 N-benzyl-N,N-bis(2-phthalimidoethyl)amine 
• 106-31-0 butanoic acid anhydride 

Relevant articles and documents

Doubly and Triply Bridged Polyoxapolyazaheterophanes Derived from 2,4,6-Trichloro-s-triazine

Doubly and triply bridged polyoxapolyazaheterophanes (1, 2) have been synthesized from 2,4,6-trichloro-s-triazine by using the different reactivity of the three chlorine atoms toward neutral nucleophiles.Introduction of alkyl groups and/or of heteroatoms in the bridging chains makes these systems soluble in organic solvents.Triazinophanes 1h and 2b, with NH groups in the bridging chains, may be used as phase-transfer catalysts in nucleophilic aliphatic substitutions. 13C NMR spectra indicate that molecules 1 and 2 either exists in a single nonsymmetric conformation up to about room temperature or, more likely, that there are two or more differently populated conformations separated by a high interconversion barrier.