940-06-7 (烟酸杂质L,3,5-Dinitropyridine)

烟酸杂质L(940-06-7)名称与标识符

名称

中文别名:
3,5-二硝基吡啶;烟酸杂质L;
英文别名:
Pyridine, 3,5-dinitro-;3,5-DINITROPYRIDINE;Nicotinic Acid Impurity L (3, 5-Dinitropyridine);3,5-Dinitro-pyridin;3,5-dinitro-pyridine;Pyridine,3,5-dinitro;3,5-Dinitropyridine (ACI);

标识符

MDL:
MFCD00234030
InChIKey:
RFSIFTKIXZLPHR-UHFFFAOYSA-N
Inchi:
1S/C5H3N3O4/c9-7(10)4-1-5(8(11)12)3-6-2-4/h1-3H
SMILES:
[O-][N+](C1C=C([N+](=O)[O-])C=NC=1)=O

烟酸杂质L(940-06-7)物化性质

实验特性

  • LogP : 1.94440
  • PSA : 104.53000

计算特性

  • 精确分子量 : 169.01200
  • 氢键供体数量 : 0
  • 氢键受体数量 : 1
  • 可旋转化学键数量 : 2
  • 重原子数量 : 12

烟酸杂质L(940-06-7)海关数据

海关编码:
2933399090
海关数据:

中国海关编码:

2933399090

概述:

2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期

Summary:

2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

烟酸杂质L(940-06-7)合成路线

合成路线:1 步
反应条件:
参考文献:
Synthesis of 3,5-dinitropyridine
Plazek, Edwin, Recueil des Travaux Chimiques des Pays-Bas et de la Belgique, 1953, 72, 569-75
合成路线:1 步
反应条件:
参考文献:
Reactions of 3-R-5-nitropyridines with nucleophiles: Nucleophilic substitution vs conjugate addition
Bastrakov, Maxim A.; Nikol'skiy, Vladislav V.; Starosotnikov, Alexey M.; Fedyanin, Ivan V.; Shevelev, Svyatoslav A.; et al, Tetrahedron, 2019, 75(47),
合成路线:1 步
反应条件:
参考文献:
3,5-Pyridyne-A Heterocyclic meta-Benzyne Derivative
Winkler, Michael; Cakir, Bayram; Sander, Wolfram, Journal of the American Chemical Society, 2004, 126(19), 6135-6149
合成路线:1 步
反应条件:
参考文献:
Electron-Deficient Heteroarenium Salts: An Organocatalytic Tool for Activation of Hydrogen Peroxide in Oxidations
Sturala, Jiri; Bohacova, Sona; Chudoba, Josef; Metelkova, Radka; Cibulka, Radek, Journal of Organic Chemistry, 2015, 80(5), 2676-2699
合成路线:1 步
反应条件:
参考文献:
Lewis Acidic Boranes, Lewis Bases, and Equilibrium Constants: A Reliable Scaffold for a Quantitative Lewis Acidity/Basicity Scale
Mayer, Robert J. ; Hampel, Nathalie; Ofial, Armin R., Chemistry - A European Journal, 2021, 27(12), 4070-4080
合成路线:1 步
反应条件:
参考文献:
Preparation of 3-(heterocyclylmethoxy)pyridines as nicotinic cholinergic agonists
, United States, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of heterocyclic ethers as neuronal nicotinic receptor ligands
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Ozone-mediated C-nitration of pyridine and methylpyridines with nitrogen dioxide
Suzuki, Hitomi; Kozai, Iku; Murashima, Takashi, Journal of Chemical Research, 1993, (4), 156-7
合成路线:1 步
参考文献:
Product class 1: pyridines
Spitzner, D., Science of Synthesis, 2005, 15, 11-284
合成路线:1 步
参考文献:
Thermal Decomposition Pathways of 1,3,3-Trinitroazetidine (TNAZ), Related 3,3-Dinitroazetidium Salts, and 15N, 13C, and 2H Isotopomers
Oxley, Jimmie; Smith, James; Zheng, Weiyi; Rogers, Evan; Coburn, Michael, Journal of Physical Chemistry A, 1997, 101(24), 4375-4383
合成路线:1 步
参考文献:
Preparation of 2-(3-pyridyloxyalkyl)azetidines and -pyrrolidines as nicotinic receptor ligands
, World Intellectual Property Organization, , ,
合成路线:1 步
参考文献:
Mineral acid-free preparation of nitro compounds from pyridine or its derivatives
, Japan, , ,
合成路线:1 步
参考文献:
Pyrimidines. LXIV. Ring transformations in reactions of heterocyclic compounds with nucleophiles. XX. Conversion of 5-nitropyrimidine into 3,5-dinitropyridine. A novel ring transformation
Van der Plas, H. C.; Jongejan, H.; Koudijs, A., Journal of Heterocyclic Chemistry, 1978, 15(3), 485-7
合成路线:1 步
反应条件:
参考文献:
Construction of 3,5-dinitrated 1,4-dihydropyridines modifiable at 1,4-positions by a reaction of β-formyl-β-nitroenamines with aldehydes
Asahara, Haruyasu; Hamada, Mai; Nakaike, Yumi; Nishiwaki, Nagatoshi, RSC Advances, 2015, 5(110), 90778-90784

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