3-Amino-N-(2-phenylethyl)benzenesulfonamide

Base Information

Chemical Name:3-Amino-N-(2-phenylethyl)benzenesulfonamide
CAS No.:303780-55-4
Molecular Formula:C₁₄H₁₆N₂O₂S
Molecular Weight:276.359
Hs Code.:
DSSTox Substance ID:DTXSID501263129
Nikkaji Number:J1.365.591J

Synonyms:3-AMINO-N-(2-PHENYLETHYL)BENZENESULFONAMIDE;SCHEMBL1937574;DTXSID501263129;AKOS000145106;303780-55-4

Suppliers and Price of 3-Amino-N-(2-phenylethyl)benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-Amino-N-(2-phenylethyl)benzenesulfonamide

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:276.09324893
Heavy Atom Count:19
Complexity:358

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCNS(=O)(=O)C2=CC=CC(=C2)N

Technology Process of 3-Amino-N-(2-phenylethyl)benzenesulfonamide

There total 3 articles about 3-Amino-N-(2-phenylethyl)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: 70.0%

: 35763-22-5
N-(2-phenylethyl)-3-nitrobenzenesulfonamide

: 303780-55-4
3-amino-N-(2-phenylethyl)benzenesulfonamide

Guidance literature:: With tin(ll) chloride; In ethyl acetate; for 2h; Heating;
DOI:10.1016/S0968-0896(00)00138-3

Reference yield:

: 64-04-0
phenethylamine

: 303780-55-4
3-amino-N-(2-phenylethyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / NMM / CH₂Cl₂ / 0 - 20 °C

2: 70 percent / SnCl₂*2H₂O / ethyl acetate / 2 h / Heating

With 4-methyl-morpholine; tin(ll) chloride; In dichloromethane; ethyl acetate; 1: Substitution / 2: Reduction;
DOI:10.1016/S0968-0896(00)00138-3

Reference yield:

: 121-51-7
3-nitrobenzenesulphonyl chloride

: 303780-55-4
3-amino-N-(2-phenylethyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / NMM / CH₂Cl₂ / 0 - 20 °C

2: 70 percent / SnCl₂*2H₂O / ethyl acetate / 2 h / Heating

With 4-methyl-morpholine; tin(ll) chloride; In dichloromethane; ethyl acetate; 1: Substitution / 2: Reduction;
DOI:10.1016/S0968-0896(00)00138-3