Brief introduction of 15833-61-1

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C5H10O2, you can also check out more blogs about15833-61-1

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. COA of Formula: C5H10O2. Introducing a new discovery about 15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol

The Negative Ion Mass Spectra of Deprotonated Carbohydrates. Part 1. The Basic Hydroxymethyl-substituted Ring Systems

Tetrahydrofuran-2-methanol and tetrahydropyran-2-methanol are models for the basic ring systems of simple carbohydrates.These compounds deprotonate, in the gas phase, principally at the HO group.The major fragmentations of these systems involve competitive losses of H2O and CH2O.Labelling (18O and 2H), and product ion studies, indicate that proton transfer between the 3-position on the ring and -CH2O- yields a 3-anion which immediately ring opens.The ring opened alkoxide may undergo proton transfers which effectively make both of the oxygens equivalent.Other tetrahydrofuran- and tetrahydropyran-methanols also undergo ring cleavage: their negative ion spectra show subtle differences.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C5H10O2, you can also check out more blogs about15833-61-1

Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem