Other grades of this product :
| 2-Thiophenemethylamine Basic information |
| 2-Thiophenemethylamine Chemical Properties |
| Boiling point | 95-99 °C/28 mmHg (lit.) | | density | 1.103 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.5670(lit.) | | Fp | 165 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Easily soluble in ethanol and Chloroform. | | pka | 8.95±0.29(Predicted) | | form | liquid | | color | Clear colorless to yellow | | Sensitive | Air Sensitive | | BRN | 106296 | | InChIKey | FKKJJPMGAWGYPN-UHFFFAOYSA-N | | CAS DataBase Reference | 27757-85-3(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Thiophenemethanamine(27757-85-3) | | EPA Substance Registry System | 2-Thiophenemethylamine (27757-85-3) |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 26-27-36/37/39-45-25 | | RIDADR | UN 3267 8/PG 2 | | WGK Germany | 3 | | Hazard Note | Corrosive | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29349990 |
| 2-Thiophenemethylamine Usage And Synthesis |
| 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.] |
| 2-Thiophenemethylamine Preparation Products And Raw materials |
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