Acetamide, N-phenyl-2-(phenylsulfonyl)-

Base Information

Chemical Name:Acetamide, N-phenyl-2-(phenylsulfonyl)-
CAS No.:38010-31-0
Molecular Formula:C₁₄H₁₃NO₃S
Molecular Weight:275.328
Hs Code.:
DSSTox Substance ID:DTXSID80404067
Nikkaji Number:J1.304.128H
Wikidata:Q82208042
Mol file:38010-31-0.mol

Synonyms:Acetamide, N-phenyl-2-(phenylsulfonyl)-;2-(benzenesulfonyl)-N-phenylacetamide;38010-31-0;DTXSID80404067;AKOS024970738;F2536-1611

Suppliers and Price of Acetamide, N-phenyl-2-(phenylsulfonyl)-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Matrix Scientific
2-(Benzenesulfonyl)-N-phenylacetamide 95%+
5g
$ 969.00

Matrix Scientific
2-(Benzenesulfonyl)-N-phenylacetamide 95%+
2.500g
$ 640.00

Matrix Scientific
2-(Benzenesulfonyl)-N-phenylacetamide 95%+
1g
$ 294.00

Total 1 raw suppliers

Chemical Property of Acetamide, N-phenyl-2-(phenylsulfonyl)-

Chemical Property:

PSA：75.11000
LogP:3.82930
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:275.06161445
Heavy Atom Count:19
Complexity:387

Purity/Quality:: 2-(Benzenesulfonyl)-N-phenylacetamide 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=O)CS(=O)(=O)C2=CC=CC=C2

Technology Process of Acetamide, N-phenyl-2-(phenylsulfonyl)-

There total 8 articles about Acetamide, N-phenyl-2-(phenylsulfonyl)- 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: 16.0%

: 108-86-1,52753-63-6
bromobenzene

: 35008-50-5
2-(phenylsulphonyl)-acetamide

: 38010-31-0
benzenesulfonyl-acetic acid anilide

Guidance literature:: With 2-Picolinic acid; copper; potassium carbonate; In N,N-dimethyl-formamide; at 110 ℃; for 48h; Sealed tube;
DOI:10.1039/d0ra01352h

Reference yield:

: 873-55-2
sodium benzenesulfonate

: 587-65-5
N-chloroacetyl-aniline

: 38010-31-0
benzenesulfonyl-acetic acid anilide

Guidance literature:: With ethanol;

Reference yield:

: 62-53-3
aniline

: 38010-31-0
benzenesulfonyl-acetic acid anilide

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 2 h / 45 - 50 °C

2: tetrabutylammonium bromide / 1,2-dimethoxy-ethane / 4 h / Heating

With tetrabutylammomium bromide; In 1,2-dimethoxyethane; acetic acid; 1: Acylation / 2: Substitution;
DOI:10.1002/1097-458x(200005)38:5<384::aid-mrc643>3.0.co;2-4