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About This Item
经验公式（希尔记法）:
C6H6FN
CAS号:
分子量:
111.12
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
方案
98%
折射率
n20/D 1.472 (lit.)
沸点
160-161 °C (lit.)
密度
1.078 g/mL at 25 °C (lit.)
SMILES字符串
Cc1ccnc(F)c1
InChI
1S/C6H6FN/c1-5-2-3-8-6(7)4-5/h2-4H,1H3
InChI key
ZBFAXMKJADVOGH-UHFFFAOYSA-N
一般描述
2-Fluoro-4-methylpyridine, also known as 2-fluoro-4-picoline, can be prepared based on Talik′s procedure from 2-amino-5-methylpyridine via diazotization. The effect of substituents on spectral properties of 2-fluoro-6-methylpyridine has been investigated based on 13C NMR, UV and IR spectral data.
应用
2-Fluoro-4-methylpyridine may be used in the preparation of:
- 2-Fluoro-4-(iodomethyl)pyridine
- 4-(4-fluorophenyl)-5-(2-fluoropyridin-4-yl)-1,3-dihydroimidazol-2-thione
- 2-fluoro-4-pyridinemethanol
- 2-fluoro-4-pyridinemethanol, 4-methylbenzenesulfonate
- 10,10-bis[(2-fluoro-4-pyridinyl)methyl]-9(10H)-anthracenone
- 2-fluoro-3-iodo-5-methylpyridine
- 2-fluoro-4-pyridinecarboxylic acid
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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.
Journal of Medicinal Chemistry, 41(23), 4615-4622 (1998)
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.
Journal of Oral Pathology & Medicine, 65(23), 7718-7722 (2000)
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.
Organic & Biomolecular Chemistry, 6(3), 437-439 (2008)
First metalation of aryl iodides: directed ortho-lithiation of iodopyridines, halogen-dance, and application to synthesis.
Rocca P, et al.
The Journal of Organic Chemistry, 58(27), 7832-7838 (1993)
The synthesis of 2-fluoro-4-and 2-fluoro-6-pyridinecarboxylic acid and derivatives.
Roe A, et al.
Journal of the American Chemical Society, 71(12), 4152-4153 (1949)
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