464899
2,6-吡啶二甲腈
97%
别名:
2,6-二氰吡啶
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关于此项目
经验公式（希尔记法）:
C7H3N3
化学文摘社编号:
分子量:
129.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-766-1
MDL number:
产品名称
2,6-吡啶二甲腈, 97%
InChI key
XNPMXMIWHVZGMJ-UHFFFAOYSA-N
InChI
1S/C7H3N3/c8-4-6-2-1-3-7(5-9)10-6/h1-3H
SMILES string
N#Cc1cccc(n1)C#N
assay
97%
form
solid
mp
123-127 °C (lit.)
functional group
nitrile
Quality Level
Application
2,6-吡啶二甲腈可用于合成双四唑和基于吡啶的三齿配体 2,6-双（α-氨基异丙基）吡啶。
General description
2,6-吡啶二甲腈是一种杂环二腈。据报道，它被红平红球菌 A4 转化为 6-氰基吡啶-2-甲酰胺。
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Synthesis and exploratory coordination chemistry of the new ditertiary carbinamine ligand 2, 6-bis (a-aminoisopropyl) pyridine.
Dahlenburg L, et al.
Inorgorganica Chimica Acta, 360(5), 1474-1481 (2007)
Vojtech Vejvoda et al.
Biotechnology letters, 29(7), 1119-1124 (2007-05-05)
2,6-Pyridinedicarbonitrile (1a) and 2,4-pyridinedicarbonitrile (2a) were hydrated by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide (1b; 83% yield) and 2-cyanopyridine-4-carboxamide (2b; 97% yield), respectively, after 10 min. After 118 h, the intermediates 1b or 2b were transformed into 2,6-pyridinedicarboxamide (1c; 35% yield)
Synthesis and characterisation of macrocycles containing both tetrazole and pyridine functionalities.
Fleming A, et al.
Tetrahedron, 67(18), 3260-3266 (2011)
Kazuhide Kamiya et al.
ChemSusChem, 13(13), 3462-3468 (2020-04-28)
In the design of solar-energy conversion electrochemical systems, it is important to consider that natural sunlight fluctuates. By taking nitrous acid photoreduction as an example, this study has shown that the reaction pathway, and hence the reaction products, dynamically respond
Jonita Stankevičiūtė et al.
Scientific reports, 6, 39129-39129 (2016-12-17)
Pyridinols and pyridinamines are important intermediates with many applications in chemical industry. The pyridine derivatives are in great demand as synthons for pharmaceutical products. Moreover, pyridines are used either as biologically active substances or as building blocks for polymers with
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