CAS 75996-29-1

5-fluorobenzene-1,3-diol

Description:

5-Fluorobenzene-1,3-diol, also known by its CAS number 75996-29-1, is an aromatic compound characterized by the presence of a fluorine atom and two hydroxyl (-OH) groups attached to a benzene ring. The fluorine substituent is located at the 5-position, while the hydroxyl groups are positioned at the 1 and 3 positions, making it a dihydroxy derivative of fluorobenzene. This compound exhibits properties typical of phenolic compounds, including potential antioxidant activity due to the presence of hydroxyl groups. It is likely to be soluble in polar solvents due to its ability to form hydrogen bonds, while its aromatic nature may impart some degree of hydrophobicity. The presence of the fluorine atom can influence the compound's reactivity and biological activity, potentially enhancing its lipophilicity and altering its interaction with biological targets. 5-Fluorobenzene-1,3-diol may have applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis, although specific applications would depend on further research and development.

Formula: C₆H₅FO₂

InChI: InChI=1/C6H5FO2/c7-4-1-5(8)3-6(9)2-4/h1-3,8-9H

SMILES: c1c(cc(cc1O)O)F

Synonyms:

• 1,3-Benzenediol, 5-fluoro-

5-Fluororesorcinol

CAS: 75996-29-1

Formula: C₆H₅FO₂

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 128.10

Ref: 3B-F1081

5-Fluorobenzene-1,3-diol

CAS: 75996-29-1

Formula: C₆H₅FO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 128.1011

Ref: IN-DA00GA91

5-Fluorobenzene-1,3-diol

CAS: 75996-29-1

5-Fluorobenzene-1,3-diol

Purity: 98%

Molecular weight: 128.10g/mol

Ref: 54-PC910226

5-Fluoro-benzene-1,3-diol

CAS: 75996-29-1

Formula: C₆H₅FO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 128.102

Ref: 10-F037809

5-Fluororesorcinol

CAS: 75996-29-1

5-Fluororesorcinol is a fluorine-containing analog of resorcinol. It is used as a topical medication for the treatment of acne, psoriasis, and other skin disorders. 5-Fluororesorcinol has been shown to inhibit the production of tyrosinase, an enzyme that catalyzes the oxidation of phenols to quinones. This process is involved in the formation of melanin and plays a role in inflammation and cell proliferation. 5-Fluororesorcinol also binds to cannabinoid receptors (CB1 and CB2) with high affinity. The molecular model for 5-fluoro resorcinol shows hydrogen bonding interactions with the hydroxyl group and fluorine atom. It also exhibits ferroelectric behavior due to its nonlinear dipole moment. The presence of two isomers (5R or 6S) may be due to steric hindrance from one or more methyl groups in the ortho

Formula: C₆H₅FO₂

Purity: Min. 95%

Molecular weight: 128.1 g/mol

Ref: 3D-ADA99629