340722-52-3

Basic information

• Product Name: 1-[[(1,1-dimethylethoxy)carbonyl]aminomethyl]-3,5-bis(aminomethyl)-2,4,6-triethylbenzene
• CAS NO: 340722-52-3
• Molecular Weight: 349.517
• Mol File: 340722-52-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-[[(1,1-dimethylethoxy)carbonyl]aminomethyl]-3,5-bis(aminomethyl)-2,4,6-triethylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[[(1,1-dimethylethoxy)carbonyl]aminomethyl]-3,5-bis(aminomethyl)-2,4,6-triethylbenzene(340722-52-3)
• EPA Substance Registry System: 1-[[(1,1-dimethylethoxy)carbonyl]aminomethyl]-3,5-bis(aminomethyl)-2,4,6-triethylbenzene(340722-52-3)

Safety Data

• Hazardous Substances Data: 340722-52-3(Hazardous Substances Data)

Upstream product

• 190779-62-5 1,3,5-tris(azidomethyl)-2,4,6-triethylbenzene 
• 190779-61-4 2,4-bis(bromomethyl)-1,3,5-triethyl benzene 
• 181058-08-2 1,3,5-tris(bromomethyl)-2,4,6-triethylbenzene 
• 102-25-0 1,3,5-triethylbenzene 
• 24424-99-5 di-tert-butyl dicarbonate 
• 149525-65-5 1,3,5-triethyl-2,4,6-tris(aminomethyl)benzene 

Relevant articles and documents

Compounds Combining a Macrocyclic Building Block and Flexible Side-Arms as Carbohydrate Receptors: Syntheses and Structure-Binding Activity Relationship Studies

A series of new representatives of compounds combining a macrocyclic building block and flexible side-arms were prepared and their ability to act as carbohydrate receptors evaluated. The target compounds were obtained by multi-step syntheses, which included the preparation of numerous precursors as well as the isolation of a large number of by-products. The structure-binding activity relationship studies comprise, in particular, the variation of the side-arms in order to demonstrate the importance of the presence of a hydrogen bond donor in these units for the effective complexation of carbohydrates. Based on the findings of our previous studies, the variation of the bridge units is limited to benzene- and pyrrole-based moieties, whereby the use of the last-mentioned bridge type was expected to produce more effective systems. This assumption was confirmed by 1H NMR titrations and isothermal titration calorimetry.

Metal triggered fluorescence sensing of citrate using a synthetic receptor

A metal containing fluorescent chemosensor was designed, synthesized, and studied for the quantification of citrate in common beverages. The sensor consists of Cu(II) bound by a 1,10-phenanthroline ligand which is attached to a bis(aminoimidazolium) recep