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Merck
모든 사진(1)

문서

N12805

Sigma-Aldrich

2-Nitrobenzyl alcohol

97%

동의어(들):

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

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모든 사진(1)

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 코드:
12352100
PubChem Substance ID:
24897478
NACRES:
NA.22

Quality Level

100

분석

97%

형태

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

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

시험 성적서(COA)

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Sigma-Aldrich

183474

2-Nitrophenethyl alcohol

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Sigma-Aldrich

122831

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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
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
Wanting Hou et al.
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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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