2-Fluoro-4-methylpyridine
2-Fluoro-4-methylpyridine structure
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Common Name | 2-Fluoro-4-methylpyridine | ||
|---|---|---|---|---|
| CAS Number | 461-87-0 | Molecular Weight | 111.117 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 161.4±20.0 °C at 760 mmHg | |
| Molecular Formula | C6H6FN | Melting Point | 160-161 °C (lit.) | |
| MSDS | Chinese USA | Flash Point | 51.4±21.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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The synthesis of 2-fluoro-4-and 2-fluoro-6-pyridinecarboxylic acid and derivatives. Roe A, et al.
J. Am. Chem. Soc. 71(12) , 4152-4153, (1949)
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The13C NMR, UV and IR spectra of 2-fluoropyridine methyl derivatives. Puszko A and Ciurla H.
Chem. Heterocycl. Comp. 35(6) , 677-687, (1999)
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2-Fluoro-4-pyridinylmethyl analogues of linopirdine as orally active acetylcholine release-enhancing agents with good efficacy and duration of action. Earl RA, et al.
J. Med. Chem. 41(23) , 4615-4622, (1998)
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Towards the improvement of the synthesis of novel 4 (5)-aryl-5 (4)-heteroaryl-2-thio-substituted imidazoles and their p38 MAP kinase inhibitory activity. Laufer S and Koch P.
Org. Biomol. Chem. 6(3) , 437-439, (2008)
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Efficient Pyridinylmethyl Functionalization: Synthesis of 10,10-Bis[(2-fluoro-4-pyridinyl)methyl]-9(10H)-anthracenone (DMP 543), an Acetylcholine Release Enhancing Agent. Pesti JA, et al.
J. Oral. Pathol. Med. 65(23) , 7718-7722, (2000)
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First metalation of aryl iodides: directed ortho-lithiation of iodopyridines, halogen-dance, and application to synthesis. Rocca P, et al.
J. Org. Chem. 58(27) , 7832-7838, (1993)
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