Chemistry:Hydroxymethyl group
From HandWiki
 Hydroxymethyl group covalently bonded to an R group
| |
| Names | |
|---|---|
| IUPAC name
Hydroxymethyl group
| |
| Other names
Methanol radical
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
PubChem CID
|
|
| |
| |
| Properties | |
| –CH 2OH | |
| Molar mass | 31.034 g·mol−1 |
| Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−9 kJ/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
| |
| Infobox references | |
Tracking categories (test):
The hydroxymethyl group is a substituent with the structural formula –CH
2–OH. It consists of a methylene bridge (–CH
2– unit) bonded to a hydroxyl group (–OH). This makes the hydroxymethyl group an alcohol. It has the identical chemical formula with the methoxy group (–O–CH
3) that differs only in the attachment site and orientation to the rest of the molecule. However, their chemical properties are different.[1][2]
Hydroxymethyl is the side chain of encoded amino acid serine.[3]
References
- ↑ NAMING ORGANIC COMPOUNDS. p. 37. https://www.kpu.ca/sites/default/files/downloads/sup08.pdf. Retrieved 2022-08-08.
- ↑ Dong, Hao; Zheng, Erjin; Niu, Zhiyin; Zhang, Xiaoyu; Lin, Yi-Yu; Jain, Priyesh; Yu, Qiuming (2020-04-15). "Hydroxymethyl-Functionalized PEDOT-MeOH:PSS for Perovskite Solar Cells". ACS Applied Materials & Interfaces 12 (15): 17571–17582. doi:10.1021/acsami.0c01756. ISSN 1944-8252. PMID 32204591.
- ↑ Perczel, András; Farkas, Ödön; Csizmadia, Imre G. (1996-01-01). "Peptide Models. 18. Hydroxymethyl Side-Chain Induced Backbone Conformational Shifts of l -Serine Amide. All ab Initio Conformers of For- l -Ser-NH 2" (in en). Journal of the American Chemical Society 118 (33): 7809–7817. doi:10.1021/ja960464q. ISSN 0002-7863. https://pubs.acs.org/doi/10.1021/ja960464q. Retrieved 2022-08-08.
External links
 |  |
