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About This Item
Linear Formula:
FC6H3(NO2)OH
CAS Number:
Molecular Weight:
157.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
solid
mp
93-95 °C (lit.)
SMILES string
Oc1ccc(c(F)c1)[N+]([O-])=O
InChI
1S/C6H4FNO3/c7-5-3-4(9)1-2-6(5)8(10)11/h1-3,9H
InChI key
CSSGKHVRDGATJL-UHFFFAOYSA-N
Application
3-Fluoro-4-nitrophenol was used in solid phase synthesis of benzimidazoles and quinoxalin-2-ones. It was also used in the synthesis of 2-hydroxy-4-[(E,E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yloxy]nitrobenzene.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Solid phase synthesis of 5, 6, 7, 8-tetrahydro-1H-imidazo [4, 5-g] quinoxalin-6-ones.
Mazurov A.
Tetrahedron Letters, 41(1), 7-10 (2000)
J G Bundy et al.
FEBS letters, 500(1-2), 31-35 (2001-07-04)
The endogenous metabolites of the coelomic fluid of the earthworm Eisenia veneta were characterised using high-resolution one-dimensional and two-dimensional 1H nuclear magnetic resonance spectroscopy. Signals from common organic acids, such as acetate, fumarate, malonate, malate, formate, and succinate, were identified
Synthesis of the farnesyl ether 2, 3, 5-trifluoro-6-hydroxy-4-[(E,E)-3,7,11-trimethyldodeca-2, 6,10-trien-1-yloxy] nitrobenzene, and related compounds containing a substituted hydroxytrifluorophenyl residue:
Marriott JH, et al.
Journal of the Chemical Society. Perkin Transactions 1, 24, 4265-4278 (2000)
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