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| | (2-FLUOROBENZYL)METHYLAMINE Basic information |
| Product Name: | (2-FLUOROBENZYL)METHYLAMINE | | Synonyms: | (2-FLUOROBENZYL)METHYLAMINE;2-FLUORO-N-METHYLBENZYLAMINE;(2-Fluorobenzyl)methylamine95%;(2-FLUOROBENZYL)METHYLAMINE 95%;(2-fluorobenZzyl)methylamine;(2-Fluorobenzyl)Methyla E 95%;(2-FLUOROBENZYL)METH;N-Methyl-o-fluorobenzylamine | | CAS: | 399-30-4 | | MF: | C8H10FN | | MW: | 139.17 | | EINECS: | | | Product Categories: | Amines;C8;Nitrogen Compounds | | Mol File: | 399-30-4.mol |  |
| | (2-FLUOROBENZYL)METHYLAMINE Chemical Properties |
| Melting point | 139-140 °C | | Boiling point | 73 °C/12 mmHg (lit.) | | density | 1.047 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.5010(lit.) | | Fp | 155 °F | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | pka | 9.05±0.10(Predicted) | | form | Liquid | | color | Colorless to tan | | Water Solubility | Slightly soluble in water. | | Sensitive | Air Sensitive | | InChI | 1S/C8H10FN/c1-10-6-7-4-2-3-5-8(7)9/h2-5,10H,6H2,1H3 | | InChIKey | AHIHZCXUWGORQO-UHFFFAOYSA-N | | SMILES | CNCc1ccccc1F |
| Hazard Codes | Xi | | Risk Statements | 36/38 | | Safety Statements | 26-36/37 | | WGK Germany | 3 | | HS Code | 2921490090 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Aquatic Chronic 3
Eye Irrit. 2
Skin Irrit. 2 |
| | (2-FLUOROBENZYL)METHYLAMINE Usage And Synthesis |
| Uses | It is used as a pharmaceutical intermediate. | | Uses | Reactant for:
- Preparation of biologically and pharmacologically active molecules
| | Synthesis | Example 4 Synthesis of N-methyl-2-fluorobenzylamine: to a stirred solution of compound 16 (135.6 mg, 0.5 mmol, 1.0 eq.) in anhydrous THF (5 mL) was slowly added LiAlH4 (38 mg, 1.0 mmol, 2.0 eq.) at 0 °C. The reaction mixture was heated to reflux and stirred for 10 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction was carefully quenched with water and subsequently extracted with ether (10 mL x 3). The target product N-methyl-2-fluorobenzylamine was isolated and purified by acid/base extraction using 2N HCl and 2N NaOH. Finally, the solvent was evaporated under reduced pressure (15 torr) to give the colorless oily product N-methyl-2-fluorobenzylamine (60 mg, 86% yield). | | References | [1] Journal of the American Chemical Society,
[2] Journal of the American Chemical Society, 2009, vol. 131, p. 7520 - 7521
[3] Patent: US2012/59179, 2012, A1. Location in patent: Page/Page column 17 |
| | (2-FLUOROBENZYL)METHYLAMINE Preparation Products And Raw materials |
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