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About This Item
Linear Formula:
CH3C6H3(NO2)F
CAS Number:
Molecular Weight:
155.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
liquid
refractive index
n20/D 1.523 (lit.)
bp
97 °C/11 mmHg (lit.)
mp
6.5-7 °C (lit.)
density
1.27 g/mL at 25 °C (lit.)
SMILES string
Cc1c(F)cccc1[N+]([O-])=O
InChI
1S/C7H6FNO2/c1-5-6(8)3-2-4-7(5)9(10)11/h2-4H,1H3
InChI key
GXPIVRKDWZKIKZ-UHFFFAOYSA-N
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General description
2-Fluoro-6-nitrotoluene undergoes reduction in the presence of stannous chloride, followed by benzoylation to yield N-(3-fluoro-o-tolyl)benzamide. 2-Fluoro-6-nitrotoluene undergoes reaction with concentrated nitric acid at 100°C to yield 2-fluoro-6-nitrobenzoic acid.
Application
2-Fluoro-6-nitrotoluene has been used in the preparation of 4-fluoroindole via Leimgruber-Batcho procedure.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
192.2 °F - closed cup
Flash Point(C)
89 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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359. Preparation of some fluoronitro-and aminofluoro-benzoic acids, and of fluoronitro-benzenes,-toluenes, and-xylenes.
Valkanas G and Hopff H.
Journal of the Chemical Society, 1925-1927 (1963)
A synthesis of (-)-indolactam V.
Semmelhack MF and Rhee H.
Tetrahedron Letters, 34(9), 1395-1398 (1993)
139. Heterocyclic fluorine compounds. Part IV. Monofluoroindazoles.
Barben IK and Suschitzky H.
Journal of the Chemical Society, 672-676 (1960)
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