CAS 20274-69-5

(4-Fluoro-3-nitrophenyl)methanol

Description:

(4-Fluoro-3-nitrophenyl)methanol is an organic compound characterized by the presence of a phenolic structure with both a fluorine and a nitro group substituted on the aromatic ring. The compound features a hydroxymethyl group (-CH2OH) attached to the aromatic system, which contributes to its reactivity and potential applications in various chemical reactions. The fluorine atom, being electronegative, can influence the compound's electronic properties, potentially enhancing its reactivity in nucleophilic substitution reactions. The nitro group, known for its electron-withdrawing properties, can further modify the compound's reactivity and stability. This compound may be utilized in the synthesis of pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Its physical properties, such as solubility and melting point, would depend on the specific interactions of the functional groups present. Safety data should be consulted for handling, as compounds with nitro groups can be sensitive and potentially hazardous. Overall, (4-Fluoro-3-nitrophenyl)methanol is a versatile compound with significant implications in chemical research and industry.

Formula: C₇H₆FNO₃

InChI: InChI=1/C7H6FNO3/c8-6-2-1-5(4-10)3-7(6)9(11)12/h1-3,10H,4H2

SMILES: c1cc(c(cc1CO)N(=O)=O)F

Synonyms:

• (4-Fluor-3-nitrophenyl)methanol
• Benzenemethanol, 4-fluoro-3-nitro-
• 4-Fluoro-3-nitrobenzyl alcohol

Benzenemethanol, 4-fluoro-3-nitro-

CAS: 20274-69-5

Formula: C₇H₆FNO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 171.1258

Ref: IN-DA0028DC

4-Fluoro-3-nitrobenzyl alcohol

CAS: 20274-69-5

4-Fluoro-3-nitrobenzyl alcohol

Purity: 98%

Molecular weight: 171.13g/mol

Ref: 54-PC502598

4-Fluoro-3-nitro-benzyl alcohol

CAS: 20274-69-5

Formula: C₇H₆FNO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 171.127

Ref: 10-F050263

4-Fluoro-3-nitrobenzyl alcohol

CAS: 20274-69-5

4-Fluoro-3-nitrobenzyl alcohol (4FNA) is a potent, orally bioavailable, and selective inhibitor of the tyrosine kinase AXL. 4FNA binds to the ATP binding site on AXL and blocks phosphorylation of its tyrosine kinase domain. This binding leads to a conformational change in the AXL protein that prevents it from interacting with downstream signaling molecules, inhibiting T cell activation.

Formula: C₇H₆FNO₃

Purity: Min. 95%

Molecular weight: 171.13 g/mol

Ref: 3D-FF10251