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Merck
CN

275352

2-羟基-5-硝基苯甲醛

98%

别名:

5-硝基水杨醛

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关于此项目

线性分子式:
HOC6H3(NO2)CHO
化学文摘社编号:
分子量:
167.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-587-0
Beilstein/REAXYS Number:
512565
MDL number:
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产品名称

2-羟基-5-硝基苯甲醛, 98%

InChI key

IHFRMUGEILMHNU-UHFFFAOYSA-N

InChI

1S/C7H5NO4/c9-4-5-3-6(8(11)12)1-2-7(5)10/h1-4,10H

SMILES string

[H]C(=O)c1cc(ccc1O)[N+]([O-])=O

assay

98%

mp

125-128 °C (lit.)

functional group

aldehyde
nitro

Quality Level

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General description

2-羟基-5-硝基苯甲醛是一种硝基芳香化合物,用于制备席夫碱配体。

已经研究了2-羟基-5-硝基苯甲醛和绿原酸(CHL)与大鼠肝葡萄糖6-磷酸酶系统组分的相互作用
无 3-硝基异构体

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

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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Anke Rüttger et al.
BioTechniques, 41(4), 469-473 (2006-10-31)
A method is described allowing the selective determination of four cathepsins (B, H, K, and L) in live cells. Adherently growing cells are incubated with partially selective substrates for each cathepsin (peptidic derivatives of 4-methoxy-beta-naphthylamine) in microtiter plates together with
W J Arion et al.
Archives of biochemistry and biophysics, 339(2), 315-322 (1997-03-15)
We have studied the interactions of chlorogenic acid (CHL) and 2-hydroxy-5-nitrobenzaldehyde (HNB) with the components of the rat hepatic glucose 6-phosphatase (Glc-6-Pase) system. CHL and HNB are competitive inhibitors of glucose 6-phosphate (Glc-6-P) hydrolysis in intact microsomes with Ki values
Synthesis, spectroscopic characterization and antimicrobial activity of mono-, bi-and tri-nuclear metal complexes of a new Schiff base ligand
Shebl M,et al.
Journal of Molecular Structure, 980, 39-50 (2010)
M A Pajares et al.
The Journal of biological chemistry, 264(12), 6804-6809 (1989-04-25)
The 11-cis-retinal binding site of rhodopsin is of great interest because it is buried in the membrane but yet must provide an environment for charged amino acids. In addition, the active-site lysine residue must be able to engage in rapid
Qing-Bin Li et al.
Acta chimica Slovenica, 64(2), 500-505 (2017-06-18)
Two mononuclear Schiff base manganese(III) complexes, [MnL(N3)(OH2)]·CH3OH (1) and [MnL(NCS)(OH2)] · H2O (2), where L is the dianionic form of N,N'-bis(5-nitrosalicylidene)ethane-1,2-diamine, have been prepared and characterized by elemental analysis, IR and UV-Vis spectroscopy and single crystal X-ray diffraction. The Mn

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