1-Bromo-4-(ethanesulfinyl)benzene

Base Information

Chemical Name:1-Bromo-4-(ethanesulfinyl)benzene
CAS No.:30506-29-7
Molecular Formula:C8H9BrOS
Molecular Weight:233.129
Hs Code.:
DSSTox Substance ID:DTXSID40550918
Nikkaji Number:J372.987G
Mol file:30506-29-7.mol

Synonyms:30506-29-7;1-Bromo-4-(ethylsulfinyl)benzene;1-Bromo-4-(ethanesulfinyl)benzene;SCHEMBL20590378;DTXSID40550918

Suppliers and Price of 1-Bromo-4-(ethanesulfinyl)benzene

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1-Bromo-4-(ethanesulfinyl)benzene

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:231.95575
Heavy Atom Count:11
Complexity:141

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCS(=O)C1=CC=C(C=C1)Br

Technology Process of 1-Bromo-4-(ethanesulfinyl)benzene

There total 4 articles about 1-Bromo-4-(ethanesulfinyl)benzene 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: 93.0%

: 30506-30-0
1-bromo-4-ethylthiobenzene

: 30506-29-7
1-bromo-4-(ethylsulfinyl)benzene

Guidance literature:: With 1,6,8-trihydroxy-3-methyl-9,10-anthraquinone; In methanol; at 20 ℃; for 6h; Irradiation;
DOI:10.1039/d0ra02702b

Reference yield: 67.0%

: 30506-30-0
1-bromo-4-ethylthiobenzene

: 26732-20-7
4-bromo-(ethylsulfonyl)benzene

: 30506-29-7
1-bromo-4-(ethylsulfinyl)benzene

Guidance literature:: With immobilised lipase B from Candida antarctica; urea hydrogen peroxide adduct; ethyl acetate; at 37 ℃; for 24h; chemoselective reaction; Enzymatic reaction;
DOI:10.1039/d0ob01966f

Reference yield:

: 106-53-6
para-bromobenzenethiol

: 26732-20-7
4-bromo-(ethylsulfonyl)benzene

: 30506-29-7
1-bromo-4-(ethylsulfinyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; sodium iodide / water / 140 °C / Microwave irradiation

2: immobilised lipase B from Candida antarctica; urea hydrogen peroxide adduct; ethyl acetate / 24 h / 37 °C / Enzymatic reaction

With immobilised lipase B from Candida antarctica; urea hydrogen peroxide adduct; potassium carbonate; ethyl acetate; sodium iodide; In water;
DOI:10.1039/d0ob01966f