4-(2-Bromoethoxy)benzenesulfonamide

Base Information

• Chemical Name: 4-(2-Bromoethoxy)benzenesulfonamide
• CAS No.: 125174-28-9
• Molecular Formula: C8H10 Br N O3 S
• Molecular Weight: 280.142
• DSSTox Substance ID: DTXSID50407166
• Wikidata: Q82212405
• Mol file: 125174-28-9.mol

Synonyms:4-(2-bromoethoxy)benzenesulfonamide;125174-28-9;4-(2-bromoethoxy)benzene-1-sulfonamide;Benzenesulfonamide, 4-(2-bromoethoxy)-;SCHEMBL7463865;DTXSID50407166;CYGFGUSYYFANTB-UHFFFAOYSA-N;MFCD07329990;AKOS001107579;4-(2-bromoethyloxy) benzenesulfonamide;CS-0234304;EN300-14062;Z96092042

Chemical Property of 4-(2-Bromoethoxy)benzenesulfonamide

Chemical Property:

• Vapor Pressure: 1.62E-07mmHg at 25°C
• Boiling Point: 427.6°Cat760mmHg
• Flash Point: 212.4°C
• PSA: 77.77000
• Density: 1.628g/cm³
• LogP: 2.88880
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 278.95648
• Heavy Atom Count: 14
• Complexity: 254

Purity/Quality:

98.5% ^*data from raw suppliers

4-(2-Bromoethoxy)benzene-1-sulfonamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1OCCBr)S(=O)(=O)N

Technology Process of 4-(2-Bromoethoxy)benzenesulfonamide

There total 1 articles about 4-(2-Bromoethoxy)benzenesulfonamide 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: 78.0%

4-(2-bromoethoxy)benzenesulfonyl chloride (167404-38-8) → 4-(2-bromo-ethoxy)-benzenesulfonamide (125174-28-9)

Guidance literature:

With ammonia; In dichloromethane; at 0 ℃; for 0.75h;

DOI:10.1016/j.ejmech.2012.02.049

Reference yield: 86.0%

pyrrolidine (123-75-1) + 4-(2-bromo-ethoxy)-benzenesulfonamide (125174-28-9) → 4-[(2-(pyrrolidin-1-yl)ethoxy)]benzenesulfonamide (1375453-69-2)

Guidance literature:

In ethanol; for 20h; Reflux;

DOI:10.1016/j.ejmech.2012.02.049

Reference yield: 64.0%

piperidine (110-89-4) + 4-(2-bromo-ethoxy)-benzenesulfonamide (125174-28-9) → 4-[(2-(piperidin-1-yl)ethoxy)]benzenesulfonamide (1110761-44-8)

Guidance literature:

In ethanol; for 20h; Reflux;

DOI:10.1016/j.ejmech.2012.02.049

upstream raw materials:

4-(2-bromoethoxy)benzenesulfonyl chloride

Downstream raw materials:

4-(2-{Methyl-[2-(4-nitro-phenyl)-ethyl]-amino}-ethoxy)-benzenesulfonamide

4-(2-{[2-(4-Amino-phenyl)-ethyl]-methyl-amino}-ethoxy)-benzenesulfonamide

4-(2-{[2-(4-Methanesulfonylamino-phenyl)-ethyl]-methyl-amino}-ethoxy)-benzenesulfonamide

4-[(2-(pyrrolidin-1-yl)ethoxy)]benzenesulfonamide