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Merck
CN

256005

吡啶-2,6-二甲醛

97%

别名:

2,6-二甲羰基萘, 2,6-双(甲酰基)吡啶, 2,6-萘二醛, 甲醛-2,6-二甲醛

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关于此项目

经验公式(希尔记法):
C7H5NO2
化学文摘社编号:
分子量:
135.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-589-6
MDL number:
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产品名称

吡啶-2,6-二甲醛, 97%

InChI key

PMWXGSWIOOVHEQ-UHFFFAOYSA-N

InChI

1S/C7H5NO2/c9-4-6-2-1-3-7(5-10)8-6/h1-5H

SMILES string

[H]C(=O)c1cccc(n1)C([H])=O

assay

97%

form

solid

bp

152-154 °C/103 mmHg (lit.)

mp

124-125 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

Quality Level

Application

2,6-甲醛二甲醛已用于制备:
  • 功能化树脂Amberlite XAD-4
  • 硼 - 二吡咯亚甲基(BODIPY)基荧光探针与N,N′-(吡啶-2,6-二基 (亚甲基))-二苯胺取代基
  • 新型N-杂环壳聚糖气凝胶衍生物

General description

2,6-吡啶二甲醛可作为各种有机化合物合成的合成砌块。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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)

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Cennet Karadaş et al.
Food chemistry, 141(2), 655-661 (2013-06-26)
The synthesis and characterization of the resin Amberlite XAD-4 functionalized with 2,6-pyridinedicarboxaldehyde and its application in an on-line system for the preconcentration of cadmium, cobalt, copper, lead and manganese prior to determination using flame atomic absorption spectrometry (FAAS) is proposed.
Muhammad Saleem et al.
Journal of fluorescence, 26(1), 11-22 (2015-11-21)
Herein, we reported the ditriazole Schiff base derivative 1 and evaluated its photophysical properties on induction of varieties of metal ions including Na(+), Ag(+), Ni(2+), Mn(2+), Pd(2+), Co(2+), Hg(2+), Cu(2+), Pb(2+), Cd(2+), Zn(2+), Sn(2+), Fe(2+), Fe(3+), Cr(3+) and Al(3+), in
Santosh Kumar et al.
International journal of biological macromolecules, 45(4), 330-337 (2009-08-12)
The novel N-heterocyclic chitosan aerogel derivatives were prepared by reacting 79% deacetylated chitosan separately with 4-pyridinecarboxaldehyde and 2,6-pyridinedicarboxaldehyde followed by subsequent solvent exchange into acetone, filteration and lyophilization. The identity of the Schiff bases was confirmed by UV-vis absorption spectroscopy
Hua Lu et al.
The journal of physical chemistry. A, 113(51), 14081-14086 (2009-12-03)
A boron-dipyrromethene (BODIPY)-based fluorescence probe with a N,N'-(pyridine-2, 6-diylbis(methylene))-dianiline substituent (1) has been prepared by condensation of 2,6-pyridinedicarboxaldehyde with 8-(4-amino)-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene and reduction by NaBH(4). The sensing properties of compound 1 toward various metal ions are investigated via fluorometric titration in
Muhammad Hanif et al.
Molecules (Basel, Switzerland), 24(2) (2019-01-19)
The present study focuses on the design and synthesis of a cage-like organic skeleton containing two triazole rings jointed via imine linkage. These molecules can act as urease inhibitors. The in-vitro urease inhibition screening results showed that the combination of

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