Acetanilide, 2-chloro-N-ethyl-4'-sulfamoyl-

Base Information

• Chemical Name: Acetanilide, 2-chloro-N-ethyl-4'-sulfamoyl-
• CAS No.: 838-16-4
• Molecular Formula: C₁₀H₁₃ClN₂O₃S
• Molecular Weight: 276.744
• DSSTox Substance ID: DTXSID60232663
• Nikkaji Number: J73.561B
• Wikidata: Q83113734
• Mol file: 838-16-4.mol

Synonyms:BRN 2700528;ACETANILIDE, 2-CHLORO-N-ETHYL-4'-SULFAMOYL-;2-Chloro-N-ethyl-4'-sulfamoyl-acetanilide;N(sup 4)-Chloroacetyl-N(sup 4)-ethylsulfanilamide;838-16-4;2-chloro-N-ethyl-N-(4-sulfamoylphenyl)acetamide;DTXSID60232663;ADAL1231630;2-Chloro-N-ethyl-4'-sulfamoylacetanilide

Chemical Property of Acetanilide, 2-chloro-N-ethyl-4'-sulfamoyl-

Chemical Property:

• Vapor Pressure: 1.28E-08mmHg at 25°C
• Boiling Point: 459.2°C at 760 mmHg
• Flash Point: 231.5°C
• Density: 1.398g/cm³
• XLogP3: 0.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 276.0335411
• Heavy Atom Count: 17
• Complexity: 358

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(C1=CC=C(C=C1)S(=O)(=O)N)C(=O)CCl

Technology Process of Acetanilide, 2-chloro-N-ethyl-4'-sulfamoyl-

There total 1 articles about Acetanilide, 2-chloro-N-ethyl-4'-sulfamoyl- 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:

→ 4-(Ethyl-chloracetyl-amino)-benzolsulfonamid (838-16-4)

Guidance literature:

N-Ethyl-N-chloracetyl-anilin, 1) Chlorsulfonsaeure, CCl4, a) 0grad, b) 100-110grad, 2) NH3, wss. Aceton; (Zwischenprodukt 4-(Ethyl-chloracetyl-amino)-benzolsulfonylchlorid nicht naeher charakterisiert);

DOI:10.1021/jm00328a034