N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide

Base Information

Chemical Name:N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide
CAS No.:101568-44-9
Molecular Formula:C₁₁H₁₄N₂O₃S
Molecular Weight:254.31
Hs Code.:
DSSTox Substance ID:DTXSID601225255
Mol file:101568-44-9.mol

Synonyms:101568-44-9;N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide;N-{4-[(allylamino)sulfonyl]phenyl}acetamide;N-[4-(prop-2-enylsulfamoyl)phenyl]acetamide;N-(4-(N-Allylsulfamoyl)phenyl)acetamide;Cambridge id 6197958;Oprea1_089089;Oprea1_247666;DTXSID601225255;BEA56844;STK408472;AKOS000383418;CCG-281955;CS-0235566;EN300-15865;AB00104103-01;N-[4-(prop-2-en-1-ylsulfamoyl)phenyl]acetamide;AN-329/12086381;N-[4-[(2-Propen-1-ylamino)sulfonyl]phenyl]acetamide;Z45529912

Suppliers and Price of N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide

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

Aronis compounds
N-{4-[(allylamino)sulfonyl]phenyl}acetamide
100mg
$ 80.00

Aaron Chemicals
N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide 95.0%
250mg
$ 399.00

Total 2 raw suppliers

Chemical Property of N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:254.07251349
Heavy Atom Count:17
Complexity:365

Purity/Quality:

99% ^*data from raw suppliers

N-{4-[(allylamino)sulfonyl]phenyl}acetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=CC=C(C=C1)S(=O)(=O)NCC=C

Technology Process of N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide

There total 1 articles about N-{4-[(prop-2-en-1-yl)sulfamoyl]phenyl}acetamide 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:

: 107-11-9,30551-89-4
1-amino-2-propene

: 121-60-8
p-acetylaminobenzenesulfonyl chloride

: 101568-44-9
N-acetyl-sulfanilic acid allylamide

Guidance literature:: With water; potassium carbonate;

Reference yield: 59.0%

: 101568-44-9
N-acetyl-sulfanilic acid allylamide

: 1208004-07-2
N-(4-(N-(2-fluoropropyl)sulfamoyl)phenyl)-acetamide

Guidance literature:: N-acetyl-sulfanilic acid allylamide; With hydrogen fluoride; antimony pentafluoride; at -20 ℃; for 0.166667h;

With water; sodium carbonate; Cooling with ice;
DOI:10.1021/ol9029287