Description

Bis(3-fluorophenyl)disulfide (CAS No. 63930-17-6) is a high-purity organosulfur compound with the molecular formula C₁₂H₈F₂S₂. This specialized chemical, also known by its IUPAC name 1-fluoro-3-[(3-fluorophenyl)disulfanyl]benzene, features a disulfide bridge linking two 3-fluorophenyl groups, making it a valuable building block in synthetic organic chemistry and materials science. Our product is rigorously tested to ensure exceptional purity and consistency, meeting the stringent requirements of pharmaceutical research, agrochemical development, and advanced material synthesis. The presence of fluorine atoms enhances its reactivity and potential for creating fluorinated derivatives with unique properties. Available in various quantities with detailed analytical certificates, this compound is ideal for researchers requiring precise and reliable reagents for their innovative projects.

Properties

• CAS Number: 63930-17-6
• Complexity: 191
• IUPAC Name: 1-fluoro-3-[(3-fluorophenyl)disulfanyl]benzene
• InChI: InChI=1S/C12H8F2S2/c13-9-3-1-5-11(7-9)15-16-12-6-2-4-10(14)8-12/h1-8H
• InChI Key: LFVFHTBHAIVNJQ-UHFFFAOYSA-N
• Exact Mass: 254.00354893
• Molecular Formula: C12H8F2S2
• Molecular Weight: 254.3
• SMILES: C1=CC(=CC(=C1)SSC2=CC=CC(=C2)F)F
• Topological: 50.6
• Monoisotopic Mass: 254.00354893
• Synonyms: 63930-17-6, bis(3-fluorophenyl)disulfide, DTXSID50372249, DTXCID60323282, 1,2-bis(3-fluorophenyl)disulfane, Bis(3-fluorophenyl) Disulfide, bis(3-fluorophenyl)disulphide, 1-fluoro-3-[(3-fluorophenyl)disulfanyl]benzene, Bis(3-fluorophenyl) disulphide, Bis-(3-fluorophenyl)disulfide, di3-fluorophenyl disulfide, Disulfide, bis(3-fluorophenyl), 3,3′-Difluorodiphenyl Disulfide, MFCD01318104, SCHEMBL577210, SBB101428, AKOS015898607, FS-4286, AC-16503, DB-054580, B3044, CS-0182173, ST50825962, A12714, 1,1′-Disulphanediylbis(3-fluorobenzene), 1,1′-Dithiobis(3-fluorobenzene)

Application

Bis(3-fluorophenyl)disulfide serves as a versatile intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceutical and agrochemical research. Its disulfide linkage enables participation in redox reactions and serves as a precursor for thiol-based derivatives. Researchers utilize this compound in the development of novel materials with tailored electronic or optical properties due to its fluorine-substituted aromatic structure. It may also find applications in polymer chemistry as a cross-linking agent or modifier for specialty resins.

Safety and Hazards

GHS Hazard Statements

• H302 (20%): Harmful if swallowed [Warning Acute toxicity, oral]
• H312 (20%): Harmful in contact with skin [Warning Acute toxicity, dermal]
• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H332 (20%): Harmful if inhaled [Warning Acute toxicity, inhalation]
• H335 (20%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (20%)
• Acute Tox. 4 (20%)
• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)
• Acute Tox. 4 (20%)
• STOT SE 3 (20%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.