329274
2-Methoxy-5-nitrophenol
98%
Synonym(s):
5-Nitroguaiacol
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All Photos(2)
About This Item
Linear Formula:
CH3OC6H3(NO2)OH
CAS Number:
Molecular Weight:
169.13
Beilstein/REAXYS Number:
2047074
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
98%
form
powder
bp
110-112 °C/1 mmHg (lit.)
mp
103-107 °C (lit.)
SMILES string
COc1ccc(cc1O)[N+]([O-])=O
InChI
1S/C7H7NO4/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4,9H,1H3
InChI key
KXKCTSZYNCDFFG-UHFFFAOYSA-N
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General description
2-Methoxy-5-nitrophenol is the substitution photoproduct formed on irradiation of 2-chloro-4-nitroanisole at 25°C in aqueous NaOH.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Gene G Wubbels et al.
The Journal of organic chemistry, 78(10), 4834-4839 (2013-05-02)
Irradiation (λ > 330 nm) of 2-chloro-4-nitroanisole (1) at 25 °C in aqueous NaOH forms three substitution photoproducts: 2-methoxy-5-nitrophenol (2), 2-chloro-4-nitrophenol (3), and 3-chloro-4-methoxyphenol (4), in chemical yields of 69.2%, 14.3%, and 16.5%. The activation energies for the elementary steps
Nenad Manevski et al.
Drug metabolism and disposition: the biological fate of chemicals, 43(1), 126-139 (2014-10-24)
Although skin is the largest organ of the human body, cutaneous drug metabolism is often overlooked, and existing experimental models are insufficiently validated. This proof-of-concept study investigated phase II biotransformation of 11 test substrates in fresh full-thickness human skin explants
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