| Chemical Properties | Clear yellow liquid |
| Uses | 2-Thiophenemethylamine can be used as areactant involved in synthesis of Triazole-linked-thiopene conjugates and a biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein. |
| Uses | 2-Thiophenemethylamine is Reactant involved in synthesis of: Triazole-linked-thiopene conjugates. It is used for biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein.It is a reactant involved in studies of organocatalyzed asymmetric reductive amination of ketones. |
| Uses | Reactant involved in synthesis of:
- Triazole-linked-thiopene conjugates for use as a biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein
- Serotonin 5-HT1A receptor antagonists which have neuroprotective affects against ischemic cell damage
- Imidazole- and piperonyl-containing thiadiazoles and pyrimidines for use as inducible oxide synthase dimerization inhibitors
- Optoelectronic segmented polyurethanes
Reactant involved in:
- Studies of organocatalyzed asymmetric reductive amination of ketones
- Metal-free aerobic oxidative coupling of amines to imines
|
| Synthesis Reference(s) | Journal of the American Chemical Society, 68, p. 1389, 1946 DOI: 10.1021/ja01211a510 |
| General Description | 2-Thiophenemethylamine is a potential ligand replacement for poly(3-hexylthiophene)/CdSe hybrid solar cells. |
| Purification Methods | Distil the amine under reduced pressure (nitrogen), from BaO, through a column packed with glass helices. The hydrochloride has m 193-194o (from EtOH/Me2CO) and the picrate has m 181-182o. [Beilstein 18 III/IV 7096.] |
