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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

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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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
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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
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