推荐产品
方案
99%
折射率
n20/D 1.525 (lit.)
沸点
76-77 °C/2 mmHg (lit.)
密度
1.059 g/mL at 25 °C (lit.)
SMILES字符串
N#CCc1ccccn1
InChI
1S/C7H6N2/c8-5-4-7-3-1-2-6-9-7/h1-3,6H,4H2
InChI key
UKVQBONVSSLJBB-UHFFFAOYSA-N
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一般描述
2-吡啶乙腈与芳香重氮盐偶联生成芳基腙。它还与活性丙二酸酯缩合生成1-氰基-3-取代的2-羟基喹啉-4-酮。2-吡啶乙腈与热乙酸酐的酰化反应已有报告。
警示用语：
Danger
危险分类
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
201.2 °F - closed cup
闪点(°C)
94 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
F S Soliman et al.
Die Pharmazie, 32(5), 278-279 (1977-05-01)
Active malonic esters condense with 2-pyridylacetonitrile giving 1-cyano-3-substituted 2-hydroxyquinolizin-4-ones. Catalytic hydrogenation of the resulting products led to the corresponding 1-cyano-3-substituted-2-hydroxy-6.7.8.9-tetrahydroquinolizin-4-ones. On the other hand, condensation of the active malonic esters with beta-aminocrotononitrile afforded 5-cyano-3-substituted-4-hydroxy-6-methylpyridine-2-ones. The IR and NMR data are
Acylation and other reactions of 2-and 4-pyridylacetonitrile.
Gutsche CD and Voges HD.
The Journal of Organic Chemistry, 32(9), 2685-2689 (1969)
Mariam Abdullah Al-Sheikh et al.
Molecules (Basel, Switzerland), 14(11), 4406-4413 (2009-11-20)
2-Pyridylacetonitrile (1) couples with aromatic diazonium salts to yield arylhydrazones 2a-c, that were shown to exist in the syn-form 2 rather than the anti-form 4. Compounds 2a,c reacted with hydroxylamine in refluxing DMF to yield the interesting 1,2,3-triazolylpyridines 6. Attempts
Amit N Pandya et al.
Tetrahedron letters, 55(50), 6922-6924 (2014-12-17)
An efficient strategy for the synthesis of indolizines from readily available starting materials via oxidative C-H functionalization and
Masazumi Tamura et al.
Nature communications, 6, 8580-8580 (2015-10-06)
Multidentate materials formed by simply mixing heterogeneous and homogeneous components are promising for construction of versatile active sites on the surface of heterogeneous compounds, however, to the best of our knowledge, there are no reports on such materials. Self-assembly of
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