1380167-26-9

Basic information

• Product Name: 1-N-Boc-7-N(3-bromopropyl)-4-N,7-N-di(2-nosyl)-4-azeheptane-1,7-diamine
• Synonyms: 1-N-Boc-7-N(3-bromopropyl)-4-N,7-N-di(2-nosyl)-4-azeheptane-1,7-diamine
• CAS NO: 1380167-26-9
• Molecular Weight: 722.635
• Mol File: 1380167-26-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-N-Boc-7-N(3-bromopropyl)-4-N,7-N-di(2-nosyl)-4-azeheptane-1,7-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-N-Boc-7-N(3-bromopropyl)-4-N,7-N-di(2-nosyl)-4-azeheptane-1,7-diamine(1380167-26-9)
• EPA Substance Registry System: 1-N-Boc-7-N(3-bromopropyl)-4-N,7-N-di(2-nosyl)-4-azeheptane-1,7-diamine(1380167-26-9)

Safety Data

• Hazardous Substances Data: 1380167-26-9(Hazardous Substances Data)

Upstream product

• 109-64-8 1,3-dibromo-propane 
• 1380167-25-8 1-N-Boc-4-N,7-N-di(2-nosyl)-4-azeheptane-1,7-diamine 
• 56-18-8 bis(3-aminopropyl)amine 

Downstream Products

• 1380167-29-2 C₃₂H₄₂N₈O₁₂S₂ 
• 1380167-27-0 C₃₁H₄₀N₁₀O₁₀S₂ 
• 1380167-30-5 C₃₈H₄₅N₇O₁₃S₂ 
• 1380167-31-6 C₃₇H₄₃N₇O₁₃S₂ 

Relevant articles and documents

B-Z transition of (dA-T)n duplexes induced by a spermine porphyrin-conjugate via an intermediate DNA conformation

The spermine conjugate of the cationic porphyrin ligand (1) selectively induced the B-Z transition of the [(dA-T)n]2 sequence at low salt concentrations. The [(dG-C)n]2 sequence was not transformed into the Z-form. The B-Z transition was induced via an intermediate DNA conformation, which was formed by the external binding and formation of an assembly of 1 onto B-DNA.