4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

Base Information

Chemical Name:4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene
CAS No.:144432-73-5
Molecular Formula:C15H15N3O4S
Molecular Weight:333.368
Hs Code.:
DSSTox Substance ID:DTXSID001153048

Synonyms:SCHEMBL8805783;CQSZZXOHFKVEHC-UHFFFAOYSA-N;DTXSID001153048;4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene;1,2,5-Thiadiazolidine, 2-(4-nitrophenyl)-5-(phenylmethyl)-, 1,1-dioxide;144432-73-5

Suppliers and Price of 4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

Supply Marketing:

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

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Chemical Property of 4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:333.07832714
Heavy Atom Count:23
Complexity:514

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(S(=O)(=O)N1CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

There total 2 articles about 4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene 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:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 144432-72-4
2-benzyl-1,2,5-thiadiazolidine 1,1-dioxide

: 144432-73-5
4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

Guidance literature:: With sodium hydride; Multistep reaction; 1.) DMF, RT, 40 min, 2.) DMF, reflux, 1 h;
DOI:10.1021/jm00045a006

Reference yield:

: 4152-09-4
N-benzylethylenediamine

: 144432-73-5
4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / sulfamide / pyridine / 16 h / Heating

2: 1.) NaH / 1.) DMF, RT, 40 min, 2.) DMF, reflux, 1 h

With sodium hydride; SULFAMIDE; In pyridine;
DOI:10.1021/jm00045a006

Reference yield:

: 144432-73-5
4-(5-Benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)nitrobenzene

: 4-(5-benzyl-1,1-dioxo-1,2,5-thiadiazolidin-2-yl)aniline hydrochloride

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In ethanol; ethyl acetate; for 0.116667h; under 1551.4 Torr;
DOI:10.1021/jm00045a006