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Merck
CN

183466

4-Nitrophenethyl alcohol

99%

Synonym(s):

2-(4-Nitrophenyl)ethanol

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About This Item

Linear Formula:
O2NC6H4CH2CH2OH
CAS Number:
Molecular Weight:
167.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-835-8
Beilstein/REAXYS Number:
1866148
MDL number:
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Product Name

4-Nitrophenethyl alcohol, 99%

InChI key

IKMXRUOZUUKSON-UHFFFAOYSA-N

InChI

1S/C8H9NO3/c10-6-5-7-1-3-8(4-2-7)9(11)12/h1-4,10H,5-6H2

SMILES string

OCCc1ccc(cc1)[N+]([O-])=O

assay

99%

bp

177 °C/16 mmHg (lit.)

mp

59-62 °C (lit.)

functional group

hydroxyl
nitro

Quality Level

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Helvetica Chimica Acta, 76, 385-385 (1993)
The Journal of Organic Chemistry, 59, 537-537 (1994)
Roni Cohen et al.
FEBS letters, 531(3), 483-488 (2002-11-19)
It is often proposed that brown rot basidiomycetes use extracellular reactive oxygen species (ROS) to accomplish the initial depolymerization of cellulose in wood, but little evidence has been presented to show that the fungi produce these oxidants in physiologically relevant
Son T Nguyen et al.
Bioorganic & medicinal chemistry, 23(9), 2024-2034 (2015-03-31)
Recently we described a novel pyranopyridine inhibitor (MBX2319) of RND-type efflux pumps of the Enterobacteriaceae. MBX2319 (3,3-dimethyl-5-cyano-8-morpholino-6-(phenethylthio)-3,4-dihydro-1H-pyrano[3,4-c]pyridine) is structurally distinct from other known Gram-negative efflux pump inhibitors (EPIs), such as 1-(1-naphthylmethyl)-piperazine (NMP), phenylalanylarginine-β-naphthylamide (PAβN), D13-9001, and the pyridopyrimidine derivatives. Here

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