2-p-Tolylethanesulfonyl chloride

Base Information

Chemical Name:2-p-Tolylethanesulfonyl chloride
CAS No.:88106-95-0
Molecular Formula:C9H11ClO2S
Molecular Weight:218.704
Hs Code.:
European Community (EC) Number:673-802-7
Mol file:88106-95-0.mol

Synonyms:2-p-tolylethanesulfonyl chloride;88106-95-0;2-p-Tolyl-ethanesulfonyl chloride;2-(4-methylphenyl)ethanesulfonyl Chloride;2-(4-methylphenyl)ethane-1-sulfonyl chloride;SCHEMBL4702032;MFCD04117460;AKOS006223418;2-(4-methylphenyl)ethane-1-sulfonylchloride;EN300-198481

Suppliers and Price of 2-p-Tolylethanesulfonyl chloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-p-tolylethanesulfonylChloride
250mg
$ 350.00

SynChem
2-p-Tolylethanesulfonyl chloride 95+%
5 g
$ 1295.00

SynChem
2-p-Tolylethanesulfonyl chloride 95+%
1 g
$ 350.00

CHESS?
MC000649:2-p-Tolyl-ethanesulfonylchloride 98
5 g
$ 1020.00

American Custom Chemicals Corporation
2-P-TOLYLETHANESULFONYL CHLORIDE 95.00%
1G
$ 1280.66

AK Scientific
2-p-Tolylethanesulfonylchloride
5g
$ 1606.00

AK Scientific
2-p-Tolylethanesulfonylchloride
500mg
$ 483.00

AHH
2-p-Tolylethanesulfonylchloride 98%
1g
$ 280.00

Total 5 raw suppliers

Chemical Property of 2-p-Tolylethanesulfonyl chloride

Chemical Property:

Melting Point:67-68°C
PSA：42.52000
LogP:3.18690
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:218.0168285
Heavy Atom Count:13
Complexity:235

Purity/Quality:

98%min ^*data from raw suppliers

2-p-tolylethanesulfonylChloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)CCS(=O)(=O)Cl

Technology Process of 2-p-Tolylethanesulfonyl chloride

There total 4 articles about 2-p-Tolylethanesulfonyl 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: 75.0%

: 35731-81-8
sodium 4-methyl-β-phenethylsulfonate

: 88106-95-0
4-methyl-β-phenethylsulfonyl chloride

Guidance literature:: With thionyl chloride; N,N-dimethyl-formamide; In benzene; for 4h; Heating;
DOI:10.1021/ja00396a039

Reference yield: 55.0%

: 6529-51-7
2-(4-methylphenyl)ethyl bromide

: 88106-95-0
4-methyl-β-phenethylsulfonyl chloride

Guidance literature:: 2-(4-methylphenyl)ethyl bromide; With potassium thioacetate; In acetonitrile; at 0 - 20 ℃; for 1h;

With hydrogenchloride; sodium chlorite; In water; acetonitrile; for 0.666667h;
DOI:10.1016/j.bmc.2017.05.040