5416-46-6

Basic information

• Product Name: pentan-3-yl hexanoate
• CAS NO: 5416-46-6
• Molecular Formula: C₁₁H₂₂O₂
• Molecular Weight: 186.2912
• Mol File: 5416-46-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 214.2°C at 760 mmHg
• Flash Point: 82.9°C
• Density: 0.87g/cm³
• Vapor Pressure: 0.158mmHg at 25°C
• Refractive Index: 1.425
• CAS DataBase Reference: pentan-3-yl hexanoate(CAS DataBase Reference)
• NIST Chemistry Reference: pentan-3-yl hexanoate(5416-46-6)
• EPA Substance Registry System: pentan-3-yl hexanoate(5416-46-6)

Safety Data

• Hazardous Substances Data: 5416-46-6(Hazardous Substances Data)

Upstream product

• 584-02-1 2-pentanol 
• 6378-65-0 n-hexyl caproate 
• 2051-49-2 n-hexanoic anhydride 
• 111-27-3 hexan-1-ol 
• 526-95-4 gluconic acid 

Relevant articles and documents

Expanding the scope of biomass-derived chemicals through tandem reactions based on oxorhenium-catalyzed deoxydehydration

New modes of DODH: Oxorhenium compounds act as deoxydehydration(DODH)/acid dual-purpose catalysts to transform biomass-derived diol substrates into a variety of commodity chemical precursors. The power of this approach is highlighted by a tandem [1,3]-OH shift/DODH of 2-ene-1,4-diols and 2,4-diene-1,6-diols, and by a DODH/esterification sequence of sugar acids to unsaturated esters for the production of polymers and plasticizers. Copyright

Ruthenium pincer-catalyzed acylation of alcohols using esters with liberation of hydrogen under neutral conditions

Acylation of secondary alcohols using non-activated esters, in particular symmetrical esters (such as ethyl acetate), is achieved under neutral conditions with the liberation of molecular hydrogen. This unprecedented, environmentally benign reaction is homogenously catalyzed by a dearomatized ruthenium pincer PNN complex. Copyright