Interesting facts
Interesting Facts about Tetrahydrofuran-2-ylmethanol
Tetrahydrofuran-2-ylmethanol, often abbreviated as THF-2-ylmethanol, is a fascinating compound with several intriguing properties and applications. Here are some interesting points to consider:
- Structure and Stability: The compound features a five-membered ring structure, which includes a tetrahydrofuran moiety. This structural characteristic contributes to its chemical reactivity and stability.
- Versatile Solvent: Tetrahydrofuran (THF) itself is a highly polar aprotic solvent, making THF-2-ylmethanol a valuable compound in organic synthesis, particularly in reactions involving lithium reagents.
- Biological Applications: Compounds related to THF are often researched for their biological activity. THF-2-ylmethanol has potential implications in pharmaceuticals, paving the way for innovative medicinal compounds.
- Precursor to Other Compounds: Tetrahydrofuran-2-ylmethanol can act as a synthetic precursor for various complex molecules, which are essential in the development of new materials and chemicals.
Chemical Behavior and Reactions
Tetrahydrofuran-2-ylmethanol exhibits interesting chemical behavior due to its hydroxyl group. This functional group enables the compound to participate in:
- Hydrogen Bonding: The hydroxyl group makes it capable of forming hydrogen bonds, enhancing its solubility in various solvents and affecting its interaction with other chemicals.
- Nucleophilic Attack: In synthetic chemistry, the compound can undergo nucleophilic reactions due to the polar nature of the ether bond, making it react readily with electrophiles.
As a chemistry student, exploring tetrahydrofuran-2-ylmethanol can open doors to understanding more about ether chemistry, solvent behaviors, and the synthesis of novel compounds. **"Understanding the building blocks of chemistry helps us to innovate and discover,"** is a mantra that resonates in the study of such versatile compounds.
Synonyms
TETRAHYDROFURFURYL ALCOHOL
97-99-4
(Tetrahydrofuran-2-yl)methanol
Tetrahydro-2-furanmethanol
oxolan-2-ylmethanol
THFA
2-Furanmethanol, tetrahydro-
Tetrahydro-2-furanylmethanol
tetrahydro furfuryl alcohol
QO Thfa
Furfuryl alcohol, tetrahydro-
Tetrahydro-2-furancarbinol
Tetrahydrofuryl carbinol
Tetrahydro-2-furfuryl alcohol
Tetrahydrofurylalkohol
Tetrahydro-2-furylmethanol
2-(Hydroxymethyl)tetrahydrofuran
tetrahydrofuran-2-ylmethanol
Tetrahydrofurfurylalkohol
FEMA No. 3056
Tetrahydrofurylmethanol
NSC 15434
Tetrahydrofurylalkohol [Czech]
CCRIS 2923
DTXSID1029128
HSDB 5314
Tetrahydrofurfurylalkohol [Czech]
EINECS 202-625-6
Oxolan-2-methanol
MFCD00005372
BRN 0102723
2-Hydroxymethyl-Tetrahydrofuran
AI3-00104
XD95821VF9
NSC-15434
DTXCID909128
CHEBI:137944
.alpha.-Tetrahydrofurfuryl alcohol
EC 202-625-6
TETRAHYDROFURFURYL ALCOHOL [MI]
TETRAHYDROFURFURYL ALCOHOL [FCC]
TETRAHYDROFURFURYL ALCOHOL [FHFI]
TETRAHYDROFURFURYL ALCOHOL [HSDB]
TETRAHYDROFURFURYL ALCOHOL, (+/-)-
93842-55-8
TETRAHYDROFURFURYLALCOHOL
TETRAHYDROFURYLALKOHOL (CZECH)
CAS-97-99-4
(oxolan-2-yl)methanol
Furanmethanol, tetrahydro-
UNII-XD95821VF9
MFCD03093085
MFCD04972320
[(2R)-tetrahydrofuran-2-yl]methanol
Thfa (van)
tetrahydrofuranmethanol
tetrahydrofuran-methanol
Tetrahydro2furancarbinol
Tetrahydro2furanmethanol
Tetrahydro2furylmethanol
2-Hydroxymethyl oxolane
tetrahydrofuran--methanol
Tetrahydro2furanylmethanol
tetrahydrofuran - methanol
tetrahydrofuran-2-methanol
2Furanmethanol, tetrahydro
Tetrahydro2furfuryl alcohol
WLN: T5OTJ B1Q
2-tetrahydrofuranyl-methanol
SCHEMBL4208
Furfuryl alcohol, tetrahydro
Qo tetrahydrofurfuryl alcohol
(tetrahydro-2furanyl)methanol
2-hydroxymethyltetrahydrofuran
tetrahydro-furan-2-ylmethanol
2-hydroxymethyl tetrahydrofuran
2(Hydroxymethyl)tetrahydrofuran
alpha-Tetrahydrofurfuryl alcohol
Tetrahydrofurfuryl alcohol, 8CI
CHEMBL2287521
rac-tetrahydrofuran-2-ylmethanol
(RS)-tetrahydrofuran-2-methanol
FEMA 3056
Tetrahydrofurfuryl alcohol, 98%
Tetrahydrofurfuryl alcohol, 99%
(tetrahydro-furan-2-yl)-methanol
Tetrahydro-2-furanmethanol; THFA
(R)-(-)-Tetrahydrofurfurylalcohol
rac-2-hydroxymethyl-tetrahydrofuran
NSC15434
Tetrahydrofurfuryl alcohol, >=98%
Furfuryl alcohol, tetrahydro-(8CI)
Tox21_201324
Tox21_303393
STL280495
AKOS000118902
AKOS016352940
CS-W004058
FT14753
SB44757
SB44818
NCGC00249026-01
NCGC00257256-01
NCGC00258876-01
TETRAHYDROFURFURYL ALCOHOL [INCI]
SY106537
SY227666
DB-016193
NS00001853
T0106
EN300-19349
Tetrahydrofurfuryl alcohol, analytical standard
D77646
Q2406741
F0001-0790
202-625-6
Solubility of Tetrahydrofuran-2-ylmethanol
Tetrahydrofuran-2-ylmethanol, also known as a diol, possesses unique solubility characteristics that make it quite interesting. Its solubility properties can be summarized as follows:
As a result, tetrahydrofuran-2-ylmethanol's specific solubility profile makes it a versatile compound in the realm of organic chemistry, showcasing both the effects of molecular structure on solubility and the critical role that solvent choice plays in chemical processes.