CAS 393-09-9

4-Fluoro-1-nitro-2-(trifluoromethyl)benzene

Description:

4-Fluoro-1-nitro-2-(trifluoromethyl)benzene, with the CAS number 393-09-9, is an aromatic compound characterized by the presence of a nitro group and a trifluoromethyl group attached to a benzene ring. This compound features a fluorine atom at the para position relative to the nitro group and a trifluoromethyl group at the ortho position. It is typically a colorless to pale yellow solid at room temperature and is known for its relatively high stability due to the resonance stabilization of the aromatic system. The presence of electronegative fluorine and nitro groups contributes to its polarity and can influence its reactivity, making it useful in various chemical syntheses and applications in pharmaceuticals and agrochemicals. Additionally, the compound may exhibit unique physical properties, such as a specific melting point and boiling point, and it is important to handle it with care due to potential toxicity and environmental impact. Proper safety measures should be observed when working with this substance in a laboratory setting.

Formula: C₇H₃F₄NO₂

InChI: InChI=1/C7H3F4NO2/c8-4-1-2-6(12(13)14)5(3-4)7(9,10)11/h1-3H

InChI key: InChIKey=WMQOSURXFLBTPC-UHFFFAOYSA-N

SMILES: C(F)(F)(F)C1=C(N(=O)=O)C=CC(F)=C1

Synonyms:

• 1-Fluoro-3-trifluoromethyl-4-nitrobenzene
• 2-Nitro-5-Fluorobenzotrifluoride
• 4-Fluoro-1-Nitro-2-(Trifluoromethyl)Benzene
• 4-Fluoro-2-(trifluoromethyl)nitrobenzene
• 4-Fluoro-6-(trifluoromethyl)nitrobenzene
• 4-Nitro-3-(trifluoromethyl)fluorobenzene
• 5-Fluoro-2-Nitro-Α,Α,Α-Trifluorotoluene
• 5-Fluoro-2-nitro(trifluoromethyl)benzene
• 5-Fluoro-2-nitro-1-trifluoromethylbenzene
• Benzene, 4-fluoro-1-nitro-2-(trifluoromethyl)-
• NSC 10304
• Toluene, α,α,α,5-tetrafluoro-2-nitro-
• 5-Fluoro-2-nitrobenzotrifluoride
• 2-TRIFLUOROMETHYL-4-FLUORONITROBENZENE
• TIMTEC-BB SBB009908
• 2-nitro-α,α,α,5-tetrafluorotoluene
• 2-NITRO-ALPHA,ALPHA,ALPHA,5-TETRAFLUOROTOLUENE
• 5-Fluoro-2-nitrobenzotrifluoride 99%
• 5-Fluoro-2-nitrobenzotrifluoride,98+%
• 5-Fluoro-2-nitrobenzotrifluoride99%

5-Fluoro-2-nitrobenzotrifluoride

CAS: 393-09-9

Formula: C₇H₃F₄NO₂

Purity: >98.0%(GC)

Color and Shape: Light yellow to Yellow to Orange clear liquid

Molecular weight: 209.10

Ref: 3B-F0497

4-Fluoro-1-nitro-2-(trifluoromethyl)benzene

CAS: 393-09-9

Formula: C₇H₃F₄NO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 209.0978

Ref: IN-DA003HS9

5-Fluoro-2-nitrobenzotrifluoride

CAS: 393-09-9

5-Fluoro-2-nitrobenzotrifluoride

Formula: C₇H₃F₄NO₂

Purity: 99%

Color and Shape: Pale Yellow Low-Melting Solid

Molecular weight: 209.10g/mol

Ref: 54-PC3952

5-Fluoro-2-nitrobenzotrifluoride

CAS: 393-09-9

5-Fluoro-2-nitrobenzotrifluoride is a triamine that stabilizes complex molecules. It has been used in the synthesis of fluorinated compounds and as a nucleophile in organic reactions. The amido group, which is present on 5-fluoro-2-nitrobenzotrifluoride, reacts with electrophilic carbon atoms to form new bonds. This type of reaction is known as an amido substitution. 5-Fluoro-2-nitrobenzotrifluoride is also able to react with sodium nitrate to form a nitro group, which can be used for the synthesis of nitro compounds. As a result, this chemical has been used as a waveguide material in the fabrication of microns and operational amplifiers.

Formula: C₇H₃F₄NO₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 209.1 g/mol

Ref: 3D-FF23382

5-Fluoro-2-nitrobenzotrifluoride

CAS: 393-09-9

Formula: C₇H₃F₄NO₂

Purity: 98%

Color and Shape: Solid, Low Melting Solid

Molecular weight: 209.1

Ref: 10-F002250

5-Fluoro-2-nitrobenzotrifluoride

Controlled Product

CAS: 393-09-9

Applications A tri-substitiuted benzene derivative used in the preparation of androgen receptor modulators and other pharmaceutical compounds.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Trump, R.P. et al.: J. Comb. Chem., 9, 107 (2007);

Formula: C₇H₃F₄NO₂

Color and Shape: Neat

Molecular weight: 209.1

Ref: TR-F594600