Fluorbenside

Base Information

• Chemical Name: Fluorbenside
• CAS No.: 405-30-1
• Molecular Formula: C₁₃H₁₀ClFS
• Molecular Weight: 252.74
• Hs Code.: 2930909090
• UNII: Q449322QX1
• DSSTox Substance ID: DTXSID6041979
• Nikkaji Number: J5.722C
• Wikidata: Q27286968
• Mol file: 405-30-1.mol

Synonyms:FLUORBENSIDE;Fluoroparacide;Fluorparacide;Fluorsulphacide;Fluorosulphacide;405-30-1;Fluorbenside [ISO];Fluorosulfacide;1-chloro-4-[(4-fluorophenyl)sulfanylmethyl]benzene;Caswell No. 183B;p-Chlorobenzyl p-fluorophenyl sulphide;p-Chlorobenzyl p-fluorophenyl sulfide;Sulfide, p-chlorobenzyl p-fluorophenyl;4-Chlorobenzyl 4'-fluorophenyl sulphide;HSDB 1539;HRS 942;4-Chlorobenzyl 4-fluorphenyl sulphide;EPA Pesticide Chemical Code 283300;1-Chloro-4-(((4-fluorophenyl)thio)methyl)benzene;4-Chlorobenzyl 4'-fluorophenyl sulfide;RD 2454;BRN 3291675;Benzene, 1-chloro-4-(((4-fluorophenyl)thio)methyl)-;UNII-Q449322QX1;Q449322QX1;Benzene, 1-chloro-4-[[(4-fluorophenyl)thio]methyl]-;C13H10ClFS;FLUORBENSIDE [HSDB];SCHEMBL166370;C13-H10-Cl-F-S;DTXSID6041979;LS-147915;4-CHLOROBENZYL 4-FLUOROPHENYL SULFIDE;1-{[(4-chlorophenyl)methyl]sulfanyl}-4-fluorobenzene;Q27286968

Chemical Property of Fluorbenside

Chemical Property:

• Vapor Pressure: 0.000122mmHg at 25°C
• Melting Point: 36oC
• Boiling Point: 345.5°C at 760 mmHg
• Flash Point: 162.8°C
• PSA: 25.30000
• Density: 1.28g/cm³
• LogP: 4.77140
• XLogP3: 4.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 252.0175773
• Heavy Atom Count: 16
• Complexity: 196

Purity/Quality:

98%min ^*data from raw suppliers

1-CHLORO-4-[(4-FLUOROPHENYL)SULFANYLMETHYL]BENZENE ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Pesticides -> Organochlorine Pesticides
• Canonical SMILES: C1=CC(=CC=C1CSC2=CC=C(C=C2)F)Cl
• Uses: (4-Chlorobenzyl)(4-fluorophenyl)sulfane is an acaricide. Acaricide.

Technology Process of Fluorbenside

There total 1 articles about Fluorbenside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

sodium 4-fluorophenylthiolate (3887-61-4) + 1-Chloro-4-(chloromethyl)benzene (104-83-6) → (4-chloro-benzyl)-(4-fluoro-phenyl)-sulfide (405-30-1)

Guidance literature:

With ethanol;

DOI:10.1017/S1092852900022045

Reference yield:

(4-chloro-benzyl)-(4-fluoro-phenyl)-sulfide (405-30-1) → (4-chloro-benzyl)-(4-fluoro-phenyl)-sulfoxide (3803-14-3)

Guidance literature:

With dihydrogen peroxide; acetic acid;

DOI:10.1017/S1092852900022045

Reference yield:

(4-chloro-benzyl)-(4-fluoro-phenyl)-sulfide (405-30-1) → (4-chloro-benzyl)-(4-fluoro-phenyl)-sulfone (3871-38-3)

Guidance literature:

With dihydrogen peroxide; acetic acid;

DOI:10.1017/S1092852900022045

upstream raw materials:

sodium 4-fluorophenylthiolate

1-Chloro-4-(chloromethyl)benzene

Downstream raw materials:

(4-chloro-benzyl)-(4-fluoro-phenyl)-sulfoxide

(4-chloro-benzyl)-(4-fluoro-phenyl)-sulfone