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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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Related Categories

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

N12805-5G:
N12805-BULK:
N12805-25G:
N12805-100G:
N12805-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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