Carbamic acid, ((methylphenylamino)sulfonyl)-, 2-chloroethyl ester

Base Information

• Chemical Name: Carbamic acid, ((methylphenylamino)sulfonyl)-, 2-chloroethyl ester
• CAS No.: 116943-59-0
• Molecular Formula: C10H13 Cl N2 O4 S
• Molecular Weight: 292.7392
• DSSTox Substance ID: DTXSID20151588
• Wikidata: Q83018069
• Mol file: 116943-59-0.mol

Synonyms:BRN 5579865;2-Chloroethyl ((methylphenylamino)sulfonyl)carbamate;Carbamic acid, ((methylphenylamino)sulfonyl)-, 2-chloroethyl ester;116943-59-0;N-(Chloro-2 ethoxycarbonyl) N'-(phenyl) N'-(methyl) sulfamide [French];N-(Chloro-2 ethoxycarbonyl) N'-(phenyl) N'-(methyl) sulfamide;DTXSID20151588;LS-50335

Chemical Property of Carbamic acid, ((methylphenylamino)sulfonyl)-, 2-chloroethyl ester

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.426g/cm³
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 292.0284558
• Heavy Atom Count: 18
• Complexity: 363

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C1=CC=CC=C1)S(=O)(=O)NC(=O)OCCCl

Technology Process of Carbamic acid, ((methylphenylamino)sulfonyl)-, 2-chloroethyl ester

There total 1 articles about Carbamic acid, ((methylphenylamino)sulfonyl)-, 2-chloroethyl ester 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: 85.0%

2-chloroethyl chlorosulfonylcarbamate (87708-19-8) + N-methylaniline (100-61-8) → N-(chloro-2 ethoxycarbonyl) N'-(phenyl) N'-(methyl) sulfamide (116943-59-0)

Guidance literature:

With triethylamine; In benzene; for 15h;

Reference yield: 90.0%

N-(chloro-2 ethoxycarbonyl) N'-(phenyl) N'-(methyl) sulfamide (116943-59-0) → N-(N'-phenyl, N'-methyl sulfamyl) oxazolidinone-2 (116943-68-1)

Guidance literature:

With triethylamine; In dichloromethane; for 15h;

Reference yield: 82.0%

diazomethane (186581-53-3,908094-01-9,334-88-3) + N-(chloro-2 ethoxycarbonyl) N'-(phenyl) N'-(methyl) sulfamide (116943-59-0) → N-methyl N-(chloro-2 ethoxycarbonyl) N'-methyl N'-(phenyl) sulfamide (116943-77-2)

Guidance literature:

In diethyl ether; dichloromethane;

upstream raw materials:

2-chloroethyl chlorosulfonylcarbamate

N-methylaniline

Downstream raw materials:

N-methyl N-(chloro-2 ethoxycarbonyl) N'-methyl N'-(phenyl) sulfamide

N-(N'-phenyl, N'-methyl sulfamyl) oxazolidinone-2

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