CHLORBENSID SULFOXIDE PESTANAL 100 MG

Base Information

• Chemical Name: CHLORBENSID SULFOXIDE PESTANAL 100 MG
• CAS No.: 7047-28-1
• Molecular Formula: C13H10 Cl2 O S
• Molecular Weight: 285.194
• Mol file: 7047-28-1.mol

Synonyms:Sulfoxide,p-chlorobenzyl p-chlorophenyl (6CI,7CI,8CI); NSC 221139

Chemical Property of CHLORBENSID SULFOXIDE PESTANAL 100 MG

Chemical Property:

• Vapor Pressure: 9.63E-08mmHg at 25°C
• Boiling Point: 446.4°C at 760 mmHg
• Flash Point: 223.8°C
• PSA: 36.28000
• Density: 1.42g/cm³
• LogP: 5.16690

Purity/Quality:

99%min ^*data from raw suppliers

Chlorbensid sulfoxide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Chlorbensid sulfoxide is an achiral sulfoxide.

Technology Process of CHLORBENSID SULFOXIDE PESTANAL 100 MG

There total 4 articles about CHLORBENSID SULFOXIDE PESTANAL 100 MG 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: 85.0%

chlorbenside (103-17-3) → (4-chloro-benzyl)-(4-chloro-phenyl)-sulfoxide (7047-28-1)

Guidance literature:

With 2,6-dicarboxypyridinium chlorochromate; In acetonitrile; at 20 ℃; for 0.25h;

DOI:10.1016/j.tetlet.2004.01.006

Reference yield:

sodium p-chlorothiophenolate (18803-44-6) → (4-chloro-benzyl)-(4-chloro-phenyl)-sulfoxide (7047-28-1)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol

2: aqueous H₂O₂; acetic acid

With ethanol; dihydrogen peroxide; acetic acid;

DOI:10.1017/S1092852900022045

Reference yield:

1-Chloro-3-chloromethyl-benzene (620-20-2,130468-19-8) → (4-chloro-benzyl)-(4-chloro-phenyl)-sulfoxide (7047-28-1)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol

2: aqueous H₂O₂; acetic acid

With ethanol; dihydrogen peroxide; acetic acid;

DOI:10.1017/S1092852900022045

upstream raw materials:

chlorbenside

1-Chloro-4-(chloromethyl)benzene

p-Chlorothiophenol

sodium p-chlorothiophenolate

Downstream raw materials:

chlorbenside

Refernces

• 1、 Nishio. "Nuclear magnetic resonance studies of sulfur compounds. II. The substituent effect on geminal coupling constants and on magnetic nonequivalence of the methylene protons of sulfoxides.". . p. 1669 - 1676. Retrieved 2007/10/12.