233277
2,6-二氟吡啶
99%
别名:
2,6-二氟吡啶
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关于此项目
经验公式（希尔记法）:
C5H3F2N
化学文摘社编号:
分子量:
115.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-152-8
Beilstein/REAXYS Number:
1422549
MDL number:
产品名称
2,6-二氟吡啶, 99%
Quality Level
InChI key
MBTGBRYMJKYYOE-UHFFFAOYSA-N
InChI
1S/C5H3F2N/c6-4-2-1-3-5(7)8-4/h1-3H
SMILES string
Fc1cccc(F)n1
assay
99%
form
liquid
refractive index
n20/D 1.437 (lit.)
bp
124.5 °C/743 mmHg (lit.)
density
1.268 g/mL at 25 °C (lit.)
functional group
fluoro
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Application
2,6-二氟吡啶通过与甲硅烷基化的1,1,1-三(4-羟苯基)乙烷发生缩聚反应，可制备聚吡啶醚。
General description
已通过结合IR和NMR光谱与计算方法，研究了二异丙基氨基锂（LDA）介导的2,6-二氟吡啶在-78°C的四氢呋喃中的邻位锂化反应。已经研究了在K2CO3存在下，各种联苯酚的双三甲基甲硅烷基衍生物与2,6-二氟吡啶在N-甲基吡咯烷酮中的缩聚反应。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
91.4 °F - closed cup
flash_point_c
33 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Lekha Gupta et al.
The Journal of organic chemistry, 78(9), 4214-4230 (2012-12-29)
Lithium diisopropylamide (LDA)-mediated ortholithiations of 2-fluoropyridine and 2,6-difluoropyridine in tetrahydrofuran at -78 °C were studied using a combination of IR and NMR spectroscopic and computational methods. Rate studies show that a substrate-assisted deaggregation of LDA dimer occurs parallel to an
Multicyclic polyethers derived from 1, 1, 1-tris (4-hydroxyphenyl) ethane and 2, 6-dihalopyridines.
Kricheldorf HR, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 42(22), 5725-5735 (2004)
Cyclic poly (pyridine ether) s by the polycondensation of 2, 6-difluoropyridine with various diphenols.
Kricheldorf HR, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 430(20), 4781-4789 (2005)
Qianglu Lin et al.
Journal of the American Chemical Society, 139(19), 6644-6653 (2017-04-22)
The use of semiconductor nanocrystal quantum dots (QDs) in optoelectronic devices typically requires postsynthetic chemical surface treatments to enhance electronic coupling between QDs and allow for efficient charge transport in QD films. Despite their importance in solar cells and infrared
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