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Merck
CN

249319

4-氨基-3-硝基苯酚

98%

别名:

4-羟基-2-硝基苯胺

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关于此项目

线性分子式:
H2NC6H3(NO2)OH
化学文摘社编号:
分子量:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-236-8
Beilstein/REAXYS Number:
2210196
MDL number:
Assay:
98%
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Quality Level

assay

98%

mp

150-154 °C (lit.)

functional group

nitro

SMILES string

Nc1ccc(O)cc1[N+]([O-])=O

InChI

1S/C6H6N2O3/c7-5-2-1-4(9)3-6(5)8(10)11/h1-3,9H,7H2

InChI key

IQXUIDYRTHQTET-UHFFFAOYSA-N

Application

4-氨基-3-硝基苯酚被用于合成苯并咪唑类因子Xa(胰蛋白酶样丝氨酸蛋白酶)抑制剂和4-(4-氨基-3-硝基苯氧基)邻苯二甲腈。它还在可见基质辅助激光解吸/电离质谱分析中被用作基质


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pictograms

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signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1A

存储类别

11 - Combustible Solids

wgk

WGK 3

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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Lorianne R Shultz et al.
Molecules (Basel, Switzerland), 25(1) (2019-12-29)
Para-, or 4-nitrophenol, and related nitroaromatics are broadly used compounds in industrial processes and as a result are among the most common anthropogenic pollutants in aqueous industrial effluent; this requires development of practical remediation strategies. Their catalytic reduction to the
Synthesis, characterization, and electrical, electrochemical and gas sensing properties of a novel cyclic borazine derivative containing three phthalocyaninato zinc (II) macrocycles.
Ozer M, et al.
Synt. Metals, 155(1), 222-231 (2005)
Z Zhao et al.
Bioorganic & medicinal chemistry letters, 10(9), 963-966 (2000-06-15)
Inhibitors based on the benzimidazole scaffold showed subnanomolar potency against Factor Xa with 500-1000-fold selectivity against thrombin and 50-100-fold selectivity against trypsin. The 2-substituent on the benzimidazole ring had a strong impact on the FXa inhibitory activity. Crystallography studies suggest



全球贸易项目编号

货号GTIN
249319-100G04061838347954
249319-25G04061825928517