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Merck
CN

N12805

2-Nitrobenzyl alcohol

97%

Synonym(s):

(2-Nitrophenyl)methanol, 2-Nitrobenzenemethanol, o-(Hydroxymethyl)nitrobenzene, o-Nitrobenzyl alcohol

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About This Item

Linear Formula:
O2NC6H4CH2OH
CAS Number:
Molecular Weight:
153.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-302-6
Beilstein/REAXYS Number:
2046649
MDL number:
Assay:
97%
Form:
solid
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Product Name

2-Nitrobenzyl alcohol, 97%

InChI

1S/C7H7NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,9H,5H2

InChI key

BWRBVBFLFQKBPT-UHFFFAOYSA-N

SMILES string

OCc1ccccc1[N+]([O-])=O

assay

97%

form

solid

bp

270 °C (lit.)

mp

69-72 °C (lit.)

Quality Level

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Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Patricia Liebhäuser et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(50), 12171-12183 (2017-04-21)
Tyrosinase model systems pinpoint pathways to translating Nature's synthetic abilities for useful synthetic catalysts. Mostly, they use N-donor ligands which mimic the histidine residues coordinating the two copper centres. Copper complexes with bis(pyrazolyl)methanes with pyridinyl or imidazolyl moieties are already
Jie Cao et al.
Oncotarget, 7(50), 82170-82184 (2016-07-02)
A combination of chemo- and photo-thermal therapy (PTT) has provided a promising efficient approach for cancer therapy. To achieve the superior synergistic chemotherapeutic effect with PTT, the development of a simple theranostic nanoplatform that can provide both cancer imaging and
Martin Gaplovsky et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 4(1), 33-42 (2004-12-24)
Irradiation of 2-nitrobenzyl alcohol (1, R = H) and 1-(2-nitrophenyl)ethanol (1, R = Me) in various solvents yields 2-nitroso benzaldehyde (4, R = H) and 2-nitroso acetophenone (4 R = Me), respectively, with quantum yields of about 60%. The mechanism
Claudia Wilfer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(49), 17639-17649 (2015-10-13)
Bis(pyrazolyl)methane ligands are excellent components of model complexes used to investigate the activity of the enzyme tyrosinase. Combining the N donors 3-tert-butylpyrazole and 1-methylimidazole results in a ligand that is capable of stabilising a (μ-η(2) :η(2) )-dicopper(II) core that resembles
Wanting Hou et al.
Molecules (Basel, Switzerland), 25(21) (2020-11-11)
Due to a strong retardation effect of o-nitrobenzyl ester on polymerization, it is still a great challenge to prepare amphiphilic block copolymers for polymersomes with a o-nitrobenzyl ester-based hydrophobic block. Herein, we present one such solution to prepare amphiphilic block

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