Orthoformic acid
Orthoformic acid or methanetriol is a hypothetical compound with the formula HC(OH)3. In this molecule, the central carbon atom is bound to one hydrogen and three hydroxyl groups.
Names | |
---|---|
Preferred IUPAC name
Methanetriol[1] | |
Other names
Orthoformic acid Trihydroxymethane | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider | |
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
CH4O3 | |
Molar mass | 64.040 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Not to be confused with methanethiol.
Orthoformic acid has not been isolated to date, and is believed to be unstable, decomposing into water and formic acid.[2]
Esters
Methanetriol esters, known as orthoformates, are well known and commercially available.[3][4] Like acetals, they are stable towards bases but easily hydrolyzed in acidic conditions to the alcohol and an ester of formic acid. They are used as mild dehydrating agent. Especially well known are trimethyl orthoformate, triethyl orthoformate, and triisopropyl orthoformate.
gollark: Weird.
gollark: ... isn't it the other way round?
gollark: In case of people picking it to be "smart".
gollark: No, I would probably just be confused by the question myself.
gollark: But *why* do people think lemons are faster than potatoes? The color?
See also
- Methanol
- Methanediol
- Orthocarbonic acid (methanetetrol)
References
- "Methanetriol - PubChem". NCBI. Retrieved 22 April 2013.
- Böhm, S., Antipova, D. and Kuthan, J. (1996), "Study of methanetriol decomposition mechanisms". International Journal of Quantum Chemistry, volume 60, pages 649–655. doi:10.1002/(SICI)1097-461X(1996)60:2<649::AID-QUA3>3.0.CO;2-X
- Peter P. T. Sah, Tsu Sheng Ma (1932), ""ESTERS OF ORTHOFORMIC ACID". J. Am. Chem. Soc., volume 54, issue 7, pages 2964–2966 doi:10.1021/ja01346a048
- H. W. Post (1943), "The Chemistry of the Aliphatic Orthoesters", Reinhold, 188 pages
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.