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Merck
CN

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:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

123-127 °C (lit.)

functional group

nitrile

SMILES string

N#Cc1cccc(n1)C#N

InChI

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

InChI key

XNPMXMIWHVZGMJ-UHFFFAOYSA-N

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。

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。


pictograms

Exclamation mark

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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)



全球贸易项目编号

货号GTIN
464899-1G04061832356686
464899-5G04061833314326