1,1,2,2-Tetrachloroethylsulfenyl chloride

Base Information

• Chemical Name: 1,1,2,2-Tetrachloroethylsulfenyl chloride
• CAS No.: 1185-09-7
• Molecular Formula: C2H Cl5 S
• Molecular Weight: 234.361
• Hs Code.: 2930909090
• European Community (EC) Number: 214-679-8
• NSC Number: 44614
• UNII: 27BXA83V63
• DSSTox Substance ID: DTXSID3051597
• Nikkaji Number: J203.444A
• Wikidata: Q27254195
• Mol file: 1185-09-7.mol

Synonyms:1185-09-7;1,1,2,2-Tetrachloroethanesulfenyl chloride;1,1,2,2-TETRACHLOROETHYLSULFENYL CHLORIDE;1,1,2,2-tetrachloroethyl thiohypochlorite;1,1,2,2-Tetrachloroethanesulphenyl chloride;Ethanesulfenyl chloride, 1,1,2,2-tetrachloro-;UNII-27BXA83V63;HSDB 5792;27BXA83V63;EINECS 214-679-8;NSC 44614;NSC-44614;NSC44614;C2HCl5S;C2-H-Cl5-S;DTXSID3051597;SCHEMBL10610793;1,2,2-Tetrachloroethylsulfenyl chloride;1,2,2-Tetrachloroethanesulfenyl chloride;1,1,2,2-tetrachloroethyl sulfenyl chloride;1,1,2,2-tetrachloroethyl-sulfenyl chloride;Ethanesulfenyl chloride,1,2,2-tetrachloro-;1,1,2,2-TETRACHLOROETHYLSULFINYL CHLORIDE;Q27254195;1,1,2,2-TETRACHLOROETHYLSULFENYL CHLORIDE [HSDB]

Chemical Property of 1,1,2,2-Tetrachloroethylsulfenyl chloride

Chemical Property:

• Vapor Pressure: 0.269mmHg at 25°C
• Boiling Point: 211.1°Cat760mmHg
• Flash Point: 84.1°C
• PSA: 25.30000
• Density: 1.763g/cm³
• LogP: 3.80850
• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 233.821210
• Heavy Atom Count: 8
• Complexity: 70.8

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Sulfur Compounds
• Canonical SMILES: C(C(SCl)(Cl)Cl)(Cl)Cl

Technology Process of 1,1,2,2-Tetrachloroethylsulfenyl chloride

There total 1 articles about 1,1,2,2-Tetrachloroethylsulfenyl chloride 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:

→ 1,1,2,2-tetrachloroethanesulphenyl chloride (1185-09-7)

Guidance literature:

Bis-(1,1,2-Trichlorethyl)-disulfid, Cl2;

Reference yield:

5-cyano-1-(2,6-dimethylphenyl)uracil (75837-73-9) + 1,1,2,2-tetrachloroethanesulphenyl chloride (1185-09-7) → 5-cyano-1-(2,6-dimethylphenyl)-3-(1,1,2,2-tetrachloroethanesulphenyl)uracil

Guidance literature:

With sodium hydroxide; In hexane; dichloromethane; water;

Reference yield:

N-[1-cyano-1-phenylethyl]methanesulfonamide (103472-19-1) + 1,1,2,2-tetrachloroethanesulphenyl chloride (1185-09-7) → N-(1,1,2,2-Tetrachloroethylthio)-2-phenyl-2-(methylsulfonamido)propionitrile (103471-77-8)

Guidance literature:

With triethylamine; In hexane; dichloromethane; ethyl acetate;

Downstream raw materials:

N-(1,1,2,2-Tetrachloroethylthio)-2-phenyl-2-(methylsulfonamido)propionitrile

N-(1,1,2,2-tetrachloroethylthio)-2-(o-chlorobenzamido)-2-methylpropionitrile

2-(o-Carbmethoxybenzamido)-N-(1,1,2,2-tetrachloroethylthio)-2-methylpropionitrile

N-cyclohexyl-N-(1,1,2,2-tetrachloroethylthio)-isopropanesulfonamide

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