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Merck
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文件

464899

Sigma-Aldrich

2,6-吡啶二甲腈

97%

别名:

2,6-二氰吡啶

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About This Item

经验公式（希尔记法）:
C7H3N3
CAS号:
2893-33-6
分子量:
129.12
EC號碼:
220-766-1
MDL號碼:
MFCD00129021
分類程式碼代碼:
12352100
PubChem物質ID:
24870229
NACRES:
NA.22

品質等級

100

化驗

97%

形狀

solid

mp

123-127 °C (lit.)

SMILES 字串

N#Cc1cccc(n1)C#N

InChI

1S/C7H3N3/c8-4-6-2-1-3-7(5-9)10-6/h1-3H

InChI 密鑰

XNPMXMIWHVZGMJ-UHFFFAOYSA-N

相关类别

一般說明

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。

應用

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。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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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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