Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]-

Base Information

Chemical Name:Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]-
CAS No.:22964-45-0
Molecular Formula:C14H22 N2 O7 S2
Molecular Weight:394.47
Hs Code.:2924299090
NSC Number:104967
DSSTox Substance ID:DTXSID90945658
Nikkaji Number:J395.065D
Wikidata:Q82923071
ChEMBL ID:CHEMBL3247504
Mol file:22964-45-0.mol

Synonyms:22964-45-0;NSC104967;NSC-104967;Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]-;3'-[Bis[2-[(methylsulfonyl)oxy]ethyl]amino]acetanilide;CHEMBL3247504;DTXSID90945658;N-[3-(Bis{2-[(methanesulfonyl)oxy]ethyl}amino)phenyl]ethanimidic acid

Suppliers and Price of Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]-

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

Total 2 raw suppliers

Chemical Property of Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]-

Chemical Property:

Vapor Pressure:5.54E-20mmHg at 25°C
Boiling Point:709.6°C at 760 mmHg
Flash Point:382.9°C
PSA：135.84000
Density:1.402g/cm³
LogP:2.63840
XLogP3:0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:10
Exact Mass:394.08684339
Heavy Atom Count:25
Complexity:585

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC(=CC=C1)N(CCOS(=O)(=O)C)CCOS(=O)(=O)C

Technology Process of Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]-

There total 1 articles about Acetamide, N-[3-[bis[2-[(methylsulfonyl)oxy]ethyl]amino]phenyl]- 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: 62.0%

: 92-02-4
N,N-bis(2-hydroxyethyl)-3-acetamidoaniline

: 124-63-0
methanesulfonyl chloride

: 22964-45-0
N,N-bis(2-(methylsulfonyloxy)ethyl)-3-acetamidoaniline

Guidance literature:: With triethylamine; In ethyl acetate; at 20 ℃; for 1h;
DOI:10.1016/j.bmcl.2010.12.052

Reference yield: 75.0%

: 22964-45-0
N,N-bis(2-(methylsulfonyloxy)ethyl)-3-acetamidoaniline

: 13686-20-9
N,N-bis(2-chloroethyl)-3-acetamidoaniline

Guidance literature:: With sodium chloride; In N,N-dimethyl-formamide; at 160 ℃; for 0.333333h;
DOI:10.1016/j.bmcl.2010.12.052

Reference yield:

: 22964-45-0
N,N-bis(2-(methylsulfonyloxy)ethyl)-3-acetamidoaniline

: 1268821-35-7
4'-(3-acetamidophenyl)spiro[indoline-1,1'-piperazin]-1-ium chloride

Guidance literature:: Multi-step reaction with 2 steps

1: sodium chloride / N,N-dimethyl-formamide / 0.33 h / 160 °C

2: sodium hydrogencarbonate / ethanol / 10 h / Reflux

With sodium hydrogencarbonate; sodium chloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2010.12.052