546321
2,6-联苯基异烟酸
97%
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关于此项目
经验公式（希尔记法）:
C18H13NO2
化学文摘社编号:
分子量:
275.30
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
97%
mp
283-286 °C (lit.)
SMILES字符串
OC(=O)c1cc(nc(c1)-c2ccccc2)-c3ccccc3
InChI
1S/C18H13NO2/c20-18(21)15-11-16(13-7-3-1-4-8-13)19-17(12-15)14-9-5-2-6-10-14/h1-12H,(H,20,21)
InChI key
PWKUURSWFJBXGO-UHFFFAOYSA-N
一般描述
2,6-Diphenylisonicotinic acid can be synthesized by reacting ethyl 2,6-diphenylisonicotinate in ethanol with KOH solution.
应用
2,6-Diphenylisonicotinic acid may be used as one of the reactants in the synthesis of 7-substituted spiro[chroman-2,4′-piperidin]-4-one derivatives and ethyl 2,6-diphenylisonicotinate (a tridentate ligand).
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
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Studies with ?-oxoalkanonitriles: Simple novel synthesis of 3-[2, 6-diaryl-4-pyridyl]-3-oxopropanenitriles.
Riyadh SM, et al.
Molecules (Basel), 13(12), 3140-3148 (2008)
Synthesis of alkynylgold (III) complexes with bis-cyclometalating ligand derived from ethyl 2, 6-diphenylisonicotinate and their structural, electrochemical, photo-and electroluminescence studies.
Au VKM, et al.
Journal of Organometallic Chemistry, 792, 109-116 (2015)
Synthesis of spiro [chroman-2, 4'-piperidin]-4-one derivatives as acetyl-CoA carboxylase inhibitors.
Shinde P, et al.
Bioorganic & Medicinal Chemistry Letters, 19(3), 949-953 (2009)
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