Dimethoxytrityl
Dimethoxytrityl, often abbreviated DMT, is a protecting group widely used for protection of the 5'-hydroxy group in nucleosides, particularly in oligonucleotide synthesis.[1]
![]() | This chemical structure or diagram's factual accuracy is disputed. Article topic compound and infobox compound combination does not make much sense, it would be like having methane infobox in Methyl article. Please discuss the issue on this diagram's talk page.See also: Wikipedia structure drawing guide. Usage: {{Disputed chem|why}} – All: Category:Disputed chemical diagrams |
![]() | |
Names | |
---|---|
IUPAC name
1-methoxy-4-[(4-methoxyphenyl)-phenylmethyl]benzene | |
Other names
| |
Identifiers | |
3D model (JSmol) |
|
PubChem CID |
|
| |
| |
Properties | |
C21H19O2 | |
Molar mass | 303.4 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
It is usually bound to a molecule, but can exist as a stable cation in solution, where it appears bright orange.[2]
References
- Krotz, Achim; Cole, Douglas; Ravikumar, Vasulinga (1999). "Dimethoxytrityl Removal in Organic Medium: Efficient Oligonucleotide Synthesis Without Chlorinated Solvents". Nucleosides and Nucleotides. 18 (6–7): 1207–1209. doi:10.1080/07328319908044664.
- "Dimethoxytrityl/DMT (Orange you glad you protected that alcohol?)". Molecule of the Day. 2006-09-05. Retrieved 2022-05-03.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.