CAS 401892-80-6

3-(pentafluoro-lambda~6~-sulfanyl)benzaldehyde

Description:

3-(Pentafluoro-lambda^6-sulfanyl)benzaldehyde is an organofluorine compound characterized by the presence of a benzaldehyde functional group and a pentafluorosulfanyl substituent. The compound features a sulfur atom bonded to five fluorine atoms, which significantly influences its chemical properties, including its reactivity and polarity. The presence of the electron-withdrawing fluorine atoms enhances the electrophilic character of the benzaldehyde, making it more reactive in nucleophilic addition reactions. Additionally, the compound's structure suggests potential applications in materials science and medicinal chemistry, particularly in the development of fluorinated compounds that exhibit unique biological activities or enhanced stability. Its high fluorine content may also impart desirable properties such as increased lipophilicity and altered solubility in various solvents. Overall, 3-(pentafluoro-lambda^6-sulfanyl)benzaldehyde is a notable compound in the field of fluorinated organic chemistry, with implications for both synthetic and applied chemistry.

Formula: C₇H₅F₅OS

InChI: InChI=1/C7H5F5OS/c8-14(9,10,11,12)7-3-1-2-6(4-7)5-13/h1-5H

SMILES: c1cc(cc(c1)S(F)(F)(F)(F)F)C=O

Synonyms:

• 3-(Pentafluoro-lambda6-sulfanyl)benzaldehyde
• 3-(Pentafluorosulfur)benzaldehyde
• 3-Sulphurpentafluorobenzaldehyde
• Sulfur, pentafluoro(3-formylphenyl)-
• Vhr Csfffff

3-(Pentafluorothio)benzaldehyde

CAS: 401892-80-6

3-(Pentafluorothio)benzaldehyde

Formula: C₇H₅F₅OS

Purity: 97%

Color and Shape: clear. almost colourless liquid

Molecular weight: 232.17g/mol

Ref: 54-PC0796

3-(Pentafluorosulfanyl)benzaldehyde

CAS: 401892-80-6

Formula: C₇H₅F₅OS

Purity: 99.0%

Color and Shape: Liquid

Molecular weight: 232.17

Ref: 10-F065154

3-Sulphurpentafluorobenzaldehyde

CAS: 401892-80-6

3-Sulphurpentafluorobenzaldehyde (3SPBF) is an optimized chiral ligand that can be used in enantioselective synthesis. 3SPBF has been shown to be a good ligand for arylboronic acids, and the enantioselectivities of this compound have been investigated with arylboronic acids. Enantioselectivity is determined by the substituent groups on the phenyl ring attached to the sulfur atom. 3SPBF has also been found to be biologically active when bound to an enzyme. The nature of these interactions are not well understood, but it is hypothesized that they occur through hydrogen bonding or hydrophobic interactions.

Formula: C₇H₅F₅OS

Purity: Min. 95%

Molecular weight: 232.17 g/mol

Ref: 3D-BRA89280