26342-09-6

Basic information

• Product Name: 6-bromohexan-1-amine
• Synonyms: 6-bromohexan-1-amine
• CAS NO: 26342-09-6
• Molecular Formula: C₆H₁₄BrN
• Molecular Weight: 180.08606
• Mol File: 26342-09-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 206.3±23.0 °C(Predicted)
• Appearance: /
• Density: 1.246±0.06 g/cm3(Predicted)
• PKA: 10.57±0.10(Predicted)
• CAS DataBase Reference: 6-bromohexan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromohexan-1-amine(26342-09-6)
• EPA Substance Registry System: 6-bromohexan-1-amine(26342-09-6)

Safety Data

• Hazardous Substances Data: 26342-09-6(Hazardous Substances Data)

Upstream product

• 24566-79-8 2-(6-bromohexyl)isoindole-1,3-dione 
• 16728-68-0 6-phenoxyhexan-1-amine 
• 629-11-8 1,6-hexanediol 
• 4048-33-3 6-amino-1-hexanol 
• 629-03-8 1 ,6-dibromohexane 
• 4286-55-9 1-bromo-6-hexanol 

Downstream Products

• 14502-43-3 8-aminooct-1-yne 
• 111-49-9 hexamethylene imine 
• 10035-10-6 hydrogen bromide 
• 32765-81-4 (6-bromohexyl)-trimethylammonium bromide 

Relevant articles and documents

Synthesis of neuraminidase-resistant sialoside-modified three-way junction DNA and its binding ability to various influenza viruses

Natural sialic acid-modified compounds are capable of targeting influenza virus hemagglutinin (HA). However, these compounds have limited inhibitory effect because natural O-glycoside bond in these compounds are prone to be cleaved by neuraminidase (NA) on the surface of viruses. In this study, we synthesized NA-resistant sialoside that included unnatural S-glycoside bonds and modified this sialoside on a three-way junction (3WJ) DNA to display complementary distribution to its binding sites on a HA trimer. This S-glycoside-containing sialoside-modified 3WJ DNA showed certain NA resistance and maintained high binding affinity. Importantly, our observations showed that substituting natural O-glycoside with unnatural S-glycoside did not affect the binding affinity of the sialoside-modified 3WJ DNA for viruses. Thus, this study is an important step forward in the development of NA-resistant sialoside derivatives for more effective detection and inhibition of infection by a broad spectrum of viruses.

Pyrrolo pyrrole diketone (DPP) quaternary ammonium salt compound and its preparation and use

The invention provides diketopyrrolopyrrole (DPP) quaternary ammonium salt compounds, which are disclosed as the structural formula in the specification, wherein N-R2 is disclosed in the specification, and R1 is Cl, Br, F, I, CF3, CN, tBu, CH3, H, 2,6-F2,

Potential antiradiation agents. I. Primary aminoalkanethiosulfuric acids.

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