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184128

Sigma-Aldrich

3-Fluoro-4-nitrophenol

99%

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About This Item

Linear Formula:
FC6H3(NO2)OH
CAS Number:
394-41-2
Molecular Weight:
157.10
EC Number:
206-895-6
MDL number:
MFCD00041251
UNSPSC Code:
12352100
PubChem Substance ID:
24851092
NACRES:
NA.22

Quality Level

100

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.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H315,H318,H335

Precautionary Statements

P261 - P280 - P305 + P351 + P338

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP3239
MKCH9928
MKBH8302V
MKBG0697V
MKBH0961V

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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)
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)
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

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