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N12805

Sigma-Aldrich

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:
612-25-9
Molecular Weight:
153.14
Beilstein:
2046649
EC Number:
210-302-6
MDL number:
MFCD00007186
UNSPSC Code:
12352100
PubChem Substance ID:
24897478
NACRES:
NA.22

Assay

97%

form

solid

bp

270 °C (lit.)

mp

69-72 °C (lit.)

SMILES string

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

InChI

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

InChI key

BWRBVBFLFQKBPT-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Jie Cao et al.
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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
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
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
Yi-Zhou Gao et al.
Applied and environmental microbiology, 86(4) (2019-12-08)
All nitroarene dioxygenases reported so far originated from Nag-like naphthalene dioxygenase of Gram-negative strains, belonging to group III of aromatic ring-hydroxylating oxygenases (RHOs). Gram-positive Rhodococcus sp. strain ZWL3NT utilizes 3-nitrotoluene (3NT) as the sole source of carbon, nitrogen, and energy
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