N-(2-aminoethyl)benzenesulfonamide

Base Information

• Chemical Name: N-(2-aminoethyl)benzenesulfonamide
• CAS No.: 42988-32-9
• Molecular Formula: C8H12N2O2S
• Molecular Weight: 200.261
• European Community (EC) Number: 851-286-6
• ChEMBL ID: CHEMBL2448846
• Nikkaji Number: J1.177.058D
• Mol file: 42988-32-9.mol

Synonyms:N-(2-aminoethyl)benzenesulfonamide;42988-32-9;aminoethyl benzenesulfonamide;SCHEMBL451810;CHEMBL2448846;JVFJSUCEQDCCAH-UHFFFAOYSA-N;N-(2-amino-ethyl)-benzenesulfonamide;AKOS000154813;CS-0252035;EN300-57582

Chemical Property of N-(2-aminoethyl)benzenesulfonamide

Chemical Property:

• Melting Point: 81-83 °C
• Boiling Point: 353.3±44.0 °C(Predicted)
• PKA: 11.21±0.10(Predicted)
• PSA: 80.57000
• Density: 1.249±0.06 g/cm3(Predicted)
• LogP: 2.09560
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 200.06194880
• Heavy Atom Count: 13
• Complexity: 227

Purity/Quality:

95% ^*data from raw suppliers

N-(2-aminoethyl)benzenesulfonamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)S(=O)(=O)NCCN

Technology Process of N-(2-aminoethyl)benzenesulfonamide

There total 7 articles about N-(2-aminoethyl)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: 100.0%

→ N-(2-aminoethyl)benzenesulfonamide (42988-32-9)

Guidance literature:

Reference yield: 97.0%

ethylenediamine (107-15-3,85404-18-8) + benzenesulfonyl chloride (98-09-9) → N-(2-aminoethyl)benzenesulfonamide (42988-32-9)

Guidance literature:

With zinc oxide-nanoparticle; at 50 ℃; for 1h; chemoselective reaction; Neat (no solvent);

DOI:10.1016/j.molcata.2011.09.010

Reference yield: 84.5%

ethylenediamine (107-15-3,85404-18-8) → N,N'-bis(phenylsulfonyl)ethylenediamine (4392-52-3) + N-(2-aminoethyl)benzenesulfonamide (42988-32-9)

Guidance literature:

In tetrahydrofuran; at 25 ℃; for 14h; Inert atmosphere;

DOI:10.1021/cc900162w

upstream raw materials:

N-(2-(phenylsulfonamido)ethyl)acetamide

2,4-dinitrophenyl benzenesulfonate

ethylenediamine

benzenesulfonyl chloride

Downstream raw materials:

N-[2-(2-Hydroxy-2-phenyl-ethylamino)-ethyl]-benzenesulfonamide

N-{2-[2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-benzenesulfonamide

3-<(2-benzenesulfonamidoethyl)amino>-1-phenoxypropan-2-ol

N-[2-{((8-hydroxyquinolin-7-yl)methyl)amino}ethyl]benzenesulfonamide

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