2-Amino-N-(phenylmethyl)benzenesulfonamide

Base Information

Chemical Name:2-Amino-N-(phenylmethyl)benzenesulfonamide
CAS No.:21639-12-3
Molecular Formula:C₁₃H₁₄N₂O₂S
Molecular Weight:262.332
Hs Code.:
DSSTox Substance ID:DTXSID401267154
Nikkaji Number:J3.413.696C

Synonyms:SCHEMBL13763413;DTXSID401267154;AKOS000161083;21639-12-3;2-Amino-N-(phenylmethyl)benzenesulfonamide

Suppliers and Price of 2-Amino-N-(phenylmethyl)benzenesulfonamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Amino-N-(phenylmethyl)benzenesulfonamide

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:262.07759887
Heavy Atom Count:18
Complexity:345

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNS(=O)(=O)C2=CC=CC=C2N

Technology Process of 2-Amino-N-(phenylmethyl)benzenesulfonamide

There total 6 articles about 2-Amino-N-(phenylmethyl)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: 85.0%

: 42060-32-2
N-benzyl-2-nitrobenzenesulfonamide

: 21639-12-3
2-amino-N-benzylbenzenesulfonamide

Guidance literature:: With tin(II) chloride dihdyrate; In ethyl acetate; for 18h; Reflux;
DOI:10.1039/d1ob00968k

Reference yield: 76.0%

: 3306-62-5
2-AMINOBENZENESULFONAMIDE

: 100-51-6,185532-71-2
benzyl alcohol

: 21639-12-3
2-amino-N-benzylbenzenesulfonamide

Guidance literature:: With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; caesium carbonate; In tert-Amyl alcohol; at 120 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.5b00824

Reference yield:

: 100-46-9
benzylamine

: 21639-12-3
2-amino-N-benzylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 2 h / 0 - 20 °C

2: tin(II) chloride dihdyrate / ethyl acetate / 18 h / Reflux

With tin(II) chloride dihdyrate; triethylamine; In dichloromethane; ethyl acetate;
DOI:10.1039/d1ob00968k