184306
3-Methoxy-4-nitrobenzoic acid
98%
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About This Item
Linear Formula:
CH3OC6H3(NO2)CO2H
CAS Number:
Molecular Weight:
197.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-793-2
MDL number:
Assay:
98%
InChI key
PWURRRRGLCVBMX-UHFFFAOYSA-N
InChI
1S/C8H7NO5/c1-14-7-4-5(8(10)11)2-3-6(7)9(12)13/h2-4H,1H3,(H,10,11)
SMILES string
COc1cc(ccc1[N+]([O-])=O)C(O)=O
assay
98%
mp
233-235 °C (lit.)
Application
3-Methoxy-4-nitrobenzoic acid was used in detection of nitroaromatic compounds by CdSe- quantum dots capped with polyamidoamine dendrimer-1,12-diaminododecane core-generation 4 nanocomposites. It was used in the synthesis of vorozole derivatives.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole and vorozole templates.
Paul M Wood et al.
ChemMedChem, 6(8), 1423-1438 (2011-05-25)
Concurrent inhibition of aromatase and steroid sulfatase (STS) may provide a more effective treatment for hormone-dependent breast cancer than monotherapy against individual enzymes, and several dual aromatase-sulfatase inhibitors (DASIs) have been reported. Three aromatase inhibitors with sub-nanomolar potency, better than
M Algarra et al.
Talanta, 83(5), 1335-1340 (2011-01-18)
The detection of nitroaromatic compounds, best known as raw materials in explosives preparations, is important in many fields including environmental science, public security and forensics. CdSe quantum dots capped with PAMAM-G(4) dendrimer were synthetized in water and used for the
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