1375797-17-3

Basic information

• Product Name: N,N-bis(2-hydroxyphenylmethyl)-N-(2-pyridylmethyl)ethane-1,2-diamine
• Synonyms: N,N-bis(2-hydroxyphenylmethyl)-N-(2-pyridylmethyl)ethane-1,2-diamine
• CAS NO: 1375797-17-3
• Molecular Weight: 363.459
• Mol File: 1375797-17-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N-bis(2-hydroxyphenylmethyl)-N-(2-pyridylmethyl)ethane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-bis(2-hydroxyphenylmethyl)-N-(2-pyridylmethyl)ethane-1,2-diamine(1375797-17-3)
• EPA Substance Registry System: N,N-bis(2-hydroxyphenylmethyl)-N-(2-pyridylmethyl)ethane-1,2-diamine(1375797-17-3)

Safety Data

• Hazardous Substances Data: 1375797-17-3(Hazardous Substances Data)

Upstream product

• 1375797-30-0 C₃₇H₄₁N₇O₁₀ 
• 1375797-29-7 C₃₇H₄₂N₆O₈ 
• 1375797-28-6 C₄₁H₄₃N₇O₁₀ 
• 1375797-27-5 C₄₁H₄₄N₆O₈ 
• 1375797-26-4 C₃₈H₄₂N₆O₁₀ 
• 1375797-25-3 C₃₈H₄₃N₅O₈ 
• 1375797-24-2 C₄₅H₄₉N₇O₁₄ 
• 1375797-23-1 C₄₅H₅₀N₆O₁₂ 
• 1375797-22-0 C₄₉H₅₁N₇O₁₄ 
• 1375797-21-9 C₄₉H₅₂N₆O₁₂ 
• 1375797-19-5 C₄₆H₅₁N₅O₁₂ 
• 3731-51-9 2-(Aminomethyl)pyridine 
• 1375797-16-2 N,N-bis(2-hydroxyphenylmethyl)-2-chloroethanamine 

Downstream Products

• 1375797-19-5 C₄₆H₅₁N₅O₁₂ 
• 1375797-20-8 C₄₆H₅₀N₆O₁₄ 
• 1375797-23-1 C₄₅H₅₀N₆O₁₂ 
• 1375797-24-2 C₄₅H₄₉N₇O₁₄ 
• 1375797-21-9 C₄₉H₅₂N₆O₁₂ 
• 1375797-28-6 C₄₁H₄₃N₇O₁₀ 
• 1375797-22-0 C₄₉H₅₁N₇O₁₄ 
• 1375797-25-3 C₃₈H₄₃N₅O₈ 
• 1375797-27-5 C₄₁H₄₄N₆O₈ 
• 1375797-29-7 C₃₇H₄₂N₆O₈ 
• 1375797-30-0 C₃₇H₄₁N₇O₁₀ 

Relevant articles and documents

A new class of bioactivable self-immolative N,O-ligands

A hexadentate ligand built on an amine-bis(phenol) skeleton with an aminal, self-immolative moiety is presented. Synthesis of the ligand is convenient and relatively high yielded. Moreover, it enables synthesis of many derivatives, both in the amino-phenol and aminal fragment (various heterocycles). Once the final hexadentate ligand is synthesized via the Katritzky reaction, it becomes prone to hydrolysis. Bioactivation by β-galactosidase cleaves the glycosylic bond and a spontaneous collapse of the aminal fragment occurs, thus leading to a pentadentate chelate. This bioactivation has been shown for pyrazole, 1,2,4-triazole and benzotriazole derivatives.