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Names | |
---|---|
IUPAC name
bis(4-methoxyphenyl)-phenylmethyl radical
| |
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).
|
Dimethoxytrityl, often abbreviated DMT, is a protecting group widely used for protection of the 5'-hydroxy group in nucleosides, particularly in oligonucleotide synthesis. [1]
It is usually bound to a molecule, but can exist as a stable cation in solution, where it appears bright orange. [2]
![]() | |
Names | |
---|---|
IUPAC name
bis(4-methoxyphenyl)-phenylmethyl radical
| |
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).
|
Dimethoxytrityl, often abbreviated DMT, is a protecting group widely used for protection of the 5'-hydroxy group in nucleosides, particularly in oligonucleotide synthesis. [1]
It is usually bound to a molecule, but can exist as a stable cation in solution, where it appears bright orange. [2]