Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)-

Base Information

Chemical Name:Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)-
CAS No.:17262-65-6
Molecular Formula:C12H18N2O5S
Molecular Weight:302.351
Hs Code.:
NSC Number:132645
DSSTox Substance ID:DTXSID50169358
Nikkaji Number:J73.554J
Wikidata:Q83039023

Synonyms:17262-65-6;Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)-;N-{4-[bis(2-hydroxyethyl)sulfamoyl]phenyl}acetamide;NSC 132645;BRN 2704943;4'-(Bis(2-hydroxyethyl)sulfamoyl)acetanilide;NSC132645;N(sub 4)-Acetil-sulfanilil-N(sub 1)-(di-beta-etanol)amide [Italian];3-14-00-02056 (Beilstein Handbook Reference);SCHEMBL622483;DTXSID50169358;KCCQFZBYCFYLGD-UHFFFAOYSA-N;N(sub 4)-Acetil-sulfanilil-N(sub 1)-(di-beta-etanol)amide;STK018850;AKOS003819822;NSC-132645;N-(4-(N,N-bis(2-hydroxyethyl)sulfamoyl)phenyl)acetamide;4-acetylamino-N,N-bis-(2-hydroxyethyl)benzenesulphonamide;N-(4-{[bis(2-hydroxyethyl)amino]sulfonyl}phenyl)acetamide;N-{4-[bis-(2-hydroxyethyl)-sulphamoyl]-phenyl}-acetamide

Suppliers and Price of Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)-

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 3 raw suppliers

Chemical Property of Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)-

Chemical Property:

Density:1.399g/cm³
XLogP3:-1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:302.09364285
Heavy Atom Count:20
Complexity:393

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)-

There total 2 articles about Acetanilide, 4'-(bis(2-hydroxyethyl)sulfamoyl)- 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: 43.0%

: 111-42-2
2,2'-iminobis[ethanol]

: 121-60-8
p-acetylaminobenzenesulfonyl chloride

: 17262-65-6
N-(4-(N,N-bis(2-hydroxyethyl)sulfamoyl)phenyl)acetamide

Guidance literature:: With sodium hydrogencarbonate; In acetone; at 20 ℃; for 3h;

Reference yield:

: 17262-65-6
N-(4-(N,N-bis(2-hydroxyethyl)sulfamoyl)phenyl)acetamide

Guidance literature:: 2 Mol 2,2'-Dihydroxy-diethylamin, 1 Mol /BRN= 746676/, Δ auf dem W.bad;

Reference yield: 72.0%

: 17262-65-6
N-(4-(N,N-bis(2-hydroxyethyl)sulfamoyl)phenyl)acetamide

: 134-32-7
1-amino-naphthalene

: 4-((4-aminonaphthalen-1-yl)diazenyl)-N,N-bis(2-hydroxyethyl)benzenesulfonamide

Guidance literature:: N-(4-(N,N-bis(2-hydroxyethyl)sulfamoyl)phenyl)acetamide; With water; sodium hydroxide; at 90 ℃; for 1h;

With hydrogenchloride; sodium nitrite; In water; at 3 - 10 ℃; pH=1;

1-amino-naphthalene; With hydrogenchloride; sodium acetate; In water;