1-Chloro-4-[(4-chlorophenyl)sulfanyl-phenylmethyl]sulfanylbenzene

Base Information

• Chemical Name: 1-Chloro-4-[(4-chlorophenyl)sulfanyl-phenylmethyl]sulfanylbenzene
• CAS No.: 25850-55-9
• Molecular Formula: C19H14 Cl2 S2
• Molecular Weight: 377.358
• NSC Number: 89494
• DSSTox Substance ID: DTXSID40293439
• Nikkaji Number: J2.861.144G
• Wikidata: Q82032165
• Mol file: 25850-55-9.mol

Synonyms:25850-55-9;1-chloro-4-[(4-chlorophenyl)sulfanyl-phenylmethyl]sulfanylbenzene;1,1'-[(Phenylmethylene)disulfanediyl]bis(4-chlorobenzene);NSC89494;DTXSID40293439;NSC-89494

Chemical Property of 1-Chloro-4-[(4-chlorophenyl)sulfanyl-phenylmethyl]sulfanylbenzene

Chemical Property:

• XLogP3: 7.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 375.9913982
• Heavy Atom Count: 23
• Complexity: 306

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(SC2=CC=C(C=C2)Cl)SC3=CC=C(C=C3)Cl

Technology Process of 1-Chloro-4-[(4-chlorophenyl)sulfanyl-phenylmethyl]sulfanylbenzene

There total 18 articles about 1-Chloro-4-[(4-chlorophenyl)sulfanyl-phenylmethyl]sulfanylbenzene 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: 94.0%

p-Chlorothiophenol (106-54-7) + benzyl alcohol (100-51-6,185532-71-2) → 1-((4-chlorophenylthio)(phenyl)methylthio)-4-chlorobenzene (25850-55-9)

Guidance literature:

With 9-(2-mesityl)-10-methylacridinium perchlorate; In acetonitrile; at 30 - 35 ℃; for 24h; Schlenk technique; Irradiation;

DOI:10.1039/d0cc02352c

Reference yield: 92.0%

phenyl N-tosyl imine (51608-60-7) + p-Chlorothiophenol (106-54-7) → 1-((4-chlorophenylthio)(phenyl)methylthio)-4-chlorobenzene (25850-55-9)

Guidance literature:

With chloro-trimethyl-silane; bismuth(III) sulfate; In dichloromethane; at 20 ℃; for 4h;

DOI:10.1039/b800066b

Reference yield: 90.0%

benzaldehyde (100-52-7) + p-Chlorothiophenol (106-54-7) → 1-((4-chlorophenylthio)(phenyl)methylthio)-4-chlorobenzene (25850-55-9)

Guidance literature:

In glycerol; at 90 ℃; for 4.5h;

DOI:10.1016/j.tetlet.2010.06.049

upstream raw materials:

benzaldehyde

p-Chlorothiophenol

4,4'-(phenylmethylene)bismorpholine

phenyl N-tosyl imine

Downstream raw materials:

(p-chlorophenylsulfinyl)(p-chlorophenylthio)phenylmethane

4-chlorophenyl benzyl sulfide

benzaldehyde

p-Chlorothiophenol

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