Ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate

Base Information

Chemical Name:Ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate
CAS No.:2642-20-8
Molecular Formula:C₁₁H₁₁FO₅S
Molecular Weight:274.27
Hs Code.:
NSC Number:166443
DSSTox Substance ID:DTXSID90304600
Wikidata:Q82050624

Synonyms:2642-20-8;ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate;NSC166443;SCHEMBL1437628;DTXSID90304600;NSC-166443

Suppliers and Price of Ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate

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

Total 5 raw suppliers

Chemical Property of Ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate

Chemical Property:

Vapor Pressure:1.13E-05mmHg at 25°C
Boiling Point:370.2°Cat760mmHg
Flash Point:177.7°C
Density:1.339g/cm³
XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:274.03112278
Heavy Atom Count:18
Complexity:412

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)CC(=O)C1=CC(=CC=C1)S(=O)(=O)F

Technology Process of Ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate

There total 2 articles about Ethyl 3-(3-fluorosulfonylphenyl)-3-oxopropanoate 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:

: 2488-51-9
2-(3-Fluorosulfonyl-benzoyl)-3-oxo-butyric acid ethyl ester

: 2642-20-8
3-(3-Fluorosulfonyl-phenyl)-3-oxo-propionic acid ethyl ester

Guidance literature:: With acetic acid; In ethanol; Heating;

Reference yield:

: 454-93-3
3-fluorosulfonyl-benzoyl chloride

: 2642-20-8
3-(3-Fluorosulfonyl-phenyl)-3-oxo-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: chloroform

2: acetic acid / ethanol / Heating

With acetic acid; In ethanol; chloroform;