| 1. | How do you pronounce " propanol " and " propanal "?
|
| 2. | This process is no longer a significant source of 1-propanol.
|
| 3. | It is an isomer of isopropanol ( 2-propanol, isopropyl alcohol ).
|
| 4. | Hexafluoro-2-propanol is a speciality solvent for some polar polymers and organic synthesis.
|
| 5. | The main developer for SU-8 is 1-methoxy-2-propanol acetate.
|
| 6. | The key step employs an unusual mixture of hexafluoro-2-propanol and trifluoroethanol as solvent.
|
| 7. | Alternate synthetic routes include treating propanol with phosphorus tribromide . or via a Hunsdiecker reaction with butyric acid.
|
| 8. | 1-Propanol was discovered in 1853 by Chancel, who obtained it by fractional distillation of fusel oil.
|
| 9. | The chemical Eschweiler-Clarke methylation of 1-amino-2-propanol using formic acid and formaldehyde.
|
| 10. | The esterification process can also be reversed ( hydrolysis ) to get propanol and hexanoic acid back from propyl hexanoate.
|