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Merck

461091

4-硝基苯甲酸

98%

别名:

p-Nitrobenzoic acid

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关于此项目

线性分子式:
O2NC6H4CO2H
化学文摘社编号:
62-23-7
分子量:
167.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24869806
EC Number:
200-526-2
Beilstein/REAXYS Number:
973593
MDL number:
MFCD00007352

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产品名称

4-硝基苯甲酸, 98%

InChI key

OTLNPYWUJOZPPA-UHFFFAOYSA-N

InChI

1S/C7H5NO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4H,(H,9,10)

SMILES string

OC(=O)c1ccc(cc1)[N+]([O-])=O

assay

98%

form

solid

mp

237-240 °C (lit.)

functional group

carboxylic acid
nitro

Quality Level

200

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相关类别

Application

4-硝基苯甲酸可用于制备化合物（I 和 III）反-M2(T(i)PB)2L2，其中 T (I) PB = 2,4,6-三异丙基苯甲酸酯：
  • 化合物 I（L = 4-硝基苯甲酸盐和 M = Mo）
  • 化合物 III（L = 4-硝基苯甲酸盐和 M2 = MoW）

General description

4-硝基苯甲酸（ p -硝基苯甲酸）是一种羧酸衍生物。参与抗生素金黄地鼠的生物合成。红外光谱分析表明，对硝基苯甲酸分子以羧酸盐的形式吸附在银粉表面。

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Repr. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 2

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
BCCN7453
BCCN3383
BCCN1899
0000306684
0000306684

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Emmanuel Chanco et al.
Bioorganic & medicinal chemistry, 22(20), 5569-5577 (2014-06-30)
AurF catalyzes the N-oxidation of p-aminobenzoic acid to p-nitrobenzoic acid in the biosynthesis of the antibiotic aureothin. Here we report the characterization of AurF under optimized conditions to explore its potential use in biocatalysis. The pH optimum of the enzyme
Diffuse reflectance infrared spectra of 4-nitrobenzoic acid and 4-cyanobenzoic acid self-assembled on fine silver particles.
Soo H, et al.
Applied Spectroscopy, 52(8) (1998)
Brian G Alberding et al.
Dalton transactions (Cambridge, England : 2003), 43(29), 11397-11403 (2014-06-17)
From the reactions between Mo2(T(i)PB)4, where T(i)PB = 2,4,6-triisopropylbenzoate and two equivalents of the carboxylic acid LH (LH = 4-nitrobenzoic acid and 4'-nitro[1,1'-biphenyl]-4-carboxylic acid) the compounds trans-M2(T(i)PB)2L2 have been prepared: I (L = 4-nitrobenzoate and M = Mo), II (L
Zhifen Lin et al.
Chemical research in toxicology, 16(10), 1365-1371 (2003-10-21)
Quantitative structure-activity relationship (QSAR) approaches are proposed in this study to predict the joint effects of mixture toxicity. The initial investigation studies the joint effects between cyanogenic toxicants and aldehydes to Photobacterium phosphoreum. Joint effects are found to result from
Li Lin et al.
Chemosphere, 78(1), 66-71 (2009-10-23)
This paper describes the microwave (MW) treatment of soil contaminated by chloramphenicol (CAP), using granular activated carbon (GAC) as MW absorbent. It was found that the addition of GAC effectively increased the temperature of soil. Large MW power and GAC
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