Ethanesulfonamide

Base Information

• Chemical Name: Ethanesulfonamide
• CAS No.: 1520-70-3
• Molecular Formula: C2H7 N O2 S
• Molecular Weight: 109.149
• Hs Code.: 2935009090
• European Community (EC) Number: 675-207-8
• NSC Number: 87899
• DSSTox Substance ID: DTXSID9061752
• Nikkaji Number: J421.576A
• ChEMBL ID: CHEMBL69291
• Mol file: 1520-70-3.mol

Synonyms:Ethanesulfonamide;1520-70-3;Ethanesulfonic acid amide;MFCD03265410;CHEMBL69291;NSC 87899;ethansulfonamid;ethyl sulfonamide;ethanesulphonamide;ethane sulfonamide;ethyl sulphonamide;NSC87899;methylmethanesulfonamide;d-ornithinehydrochloride;EtSO2NH2;methyl-methanesulfonamide;SCHEMBL28038;DTXSID9061752;AMY33485;BDBM50044315;NSC-87899;AKOS000147712;CS-W003034;AS-17321;SY016774;FT-0693274;EN300-75234;J-008881;J-520439;Z54886646

Chemical Property of Ethanesulfonamide

Chemical Property:

• Vapor Pressure: 0.152mmHg at 25°C
• Melting Point: 60 °C
• Refractive Index: 1.462
• Boiling Point: 214.9 °C at 760 mmHg
• PKA: 10.81±0.60(Predicted)
• Flash Point: 83.7 °C
• PSA: 68.54000
• Density: 1.265 g/cm³
• LogP: 1.07590
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: -0.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 109.01974964
• Heavy Atom Count: 6
• Complexity: 108

Purity/Quality:

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

Ethanesulfonamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCS(=O)(=O)N

Technology Process of Ethanesulfonamide

There total 8 articles about Ethanesulfonamide 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: 99.6%

→ Ethanesulfonamide (1520-70-3)

Guidance literature:

Reference yield: 92.0%

N-(t-Butyl)ethanesulfonamide (89556-99-0) → Ethanesulfonamide (1520-70-3)

Guidance literature:

With trifluoroacetic acid; for 24h; Ambient temperature;

DOI:10.1021/jo00184a006

Reference yield: 88.0%

Ethanesulfonyl chloride (594-44-5) → Ethanesulfonamide (1520-70-3)

Guidance literature:

With ammonium hydroxide; In chloroform; for 2h; Ambient temperature;

DOI:10.1021/jo00070a026

upstream raw materials:

Ethanesulfonyl chloride

ethyl methyl sulfone

N-(t-Butyl)ethanesulfonamide

methanesulfonamide

Downstream raw materials:

N-Trimethylsilyl Ethanesulfonamide

α-Aethan-sulfamido-diphenylmethan

C₁₄H₂₃N₄O₆PS₂

N-cyclohexylethanesulfonamide

Refernces

• 1、 Vidigal, Antonio E.C.,Rubinger, Mayura M.M.,de Queiroz, Luan F.,da Silva, Lucas F.,Zambolim, Laércio,Guilardi, Silvana,Souza, Rafael A.C.,Ellena, Javier,Wetler, Emiliana B.,Oliveira, Marcelo R.L.. "Nickel complexes with phosphines and N-R-sulfonyldithiocarbimates ligands: New antifungals for the control of Hemileia vastatrix and Phakopsora pachyrhizi". . p. 724 - 732. Retrieved 2019.
• 2、 Tavares, Eder C.,Rubinger, Mayura M.M.,Zacchi, Carlos H.C.,Silva, Simone A.,Oliveira, Marcelo R.L.,Guilardi, Silvana,Alcantara, Ant?nio F. De C.,Piló-Veloso, Dorila,Zambolim, Laércio. "Synthesis, characterization, and antifungal activity of novel (Z)-N-(2-cyano-3-phenylprop-2-en-1-yl)-alkyl/aryl-sulfonamides derived from a Morita-Baylis-Hillman adduct". . p. 43 - 51. Retrieved 2014/04/17.