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经验公式(希尔记法):
C4H4N2
化学文摘社编号:
分子量:
80.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-027-6
Beilstein/REAXYS Number:
103905
MDL number:
产品名称
吡嗪, ≥99%
InChI key
KYQCOXFCLRTKLS-UHFFFAOYSA-N
InChI
1S/C4H4N2/c1-2-6-4-3-5-1/h1-4H
SMILES string
c1cnccn1
assay
≥99%
form
crystals
bp
115-116 °C (lit.)
mp
50-56 °C (lit.)
density
1.031 g/mL at 25 °C (lit.)
Quality Level
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Application
吡嗪可用于:
- 作为铜(II)线性链配位配合物合成中的桥联配体。
- 制备Cu(I)衍生的配位聚合物,其可用于金属有机骨架(MOF)的合成。
General description
吡嗪为一种1,4-二嗪,以及在几种天然产物、API、农药和功能材料中发现的一种缺电子的N-杂芳烃。
signalword
Danger
hcodes
Hazard Classifications
Flam. Sol. 1
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
131.0 °F - closed cup
flash_point_c
55 °C - closed cup
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Microwave assisted hydrothermal synthesis of a novel CuI-sulfate-pyrazine MOF
Amo-Ochoa P, et al.
Inorganic Chemistry Communications, 10(8), 921-924 (2007)
Direct C-H photoarylation of diazines using aryldiazonium salts and visible-light
Silva RC, et al.
Royal Society of Chemistry Advances, 10(52), 31115-31122 (2020)
Pyrazine-bridged Cu (ii) chains: diaquabis (n-methyl-2-pyridone) copper (ii) perchlorate complexes
Kirkman-Davis E, et al.
Dalton Transactions, 49(39), 13693-13703 (2020)
Oleg V Larionov et al.
Organic letters, 16(3), 864-867 (2014-01-15)
A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of copper catalysis and activation by lithium fluoride or magnesium chloride. The utility of this method
Nicole Favreau-Farhadi et al.
Journal of food science, 80(10), C2140-C2146 (2015-09-27)
Rosmarinic acid and Epigallocatechin gallate concentrations were studied as natural inhibitors of Maillard browning in glucose/glycine model systems, and in bakery rolls and applesauce. The concentrations of the inhibitors were varied to determine the highest level of inhibition without a
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