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| | (R)-(+)-1-(4-Methoxyphenyl)ethylamine Basic information |
| | (R)-(+)-1-(4-Methoxyphenyl)ethylamine Chemical Properties |
| Melting point | <-20°C | | Boiling point | 65°C 0,4mm | | alpha | 32 º (neat) | | density | 1.024 g/mL at 20 °C(lit.) | | refractive index | n20/D 1.533 | | Fp | 65°C/0.38mm | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | liquid | | pka | 9.29±0.10(Predicted) | | Water Solubility | Soluble in water (10g/L). | | Sensitive | Air Sensitive | | BRN | 2413029 | | InChIKey | JTDGKQNNPKXKII-SSDOTTSWSA-N | | CAS DataBase Reference | 22038-86-4(CAS DataBase Reference) |
| Hazard Codes | C | | Risk Statements | 34-22 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 2735 8/PG 3 | | WGK Germany | 3 | | F | 10-34 | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29222990 |
| | (R)-(+)-1-(4-Methoxyphenyl)ethylamine Usage And Synthesis |
| Chemical Properties | Colorless liquid | | Uses | (R)-(+)-4-Methoxy-α-methylbenzylamine can be used as a reactant to prepare:
- Enantiopure stereoisomers of hemicryptophanes, which are used for the recognition of glucopyranosides.
- Bicyclic Geissman-Waiss lactone via intramolecular ring-closure reaction of the diastereomeric mixture of sulfonium salts.
- N-[(1R)-1-(4-Methoxyphenyl)ethyl]-N′-methylthiourea by reacting with methyl isothiocyanate.
| | Uses | (R)-(+)-1-(4-Methoxyphenyl)ethylamine use in diastereo-and enantioselective Michael addition reactions. Thiazoles has been prepared from (R)-(+)-1-(4-Methoxyphenyl)ethylamine. |
| | (R)-(+)-1-(4-Methoxyphenyl)ethylamine Preparation Products And Raw materials |
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