2-Nitro-N-[6-(1,3-thiazolidin-3-YL)hexyl]benzamide

Base Information

Chemical Name:2-Nitro-N-[6-(1,3-thiazolidin-3-YL)hexyl]benzamide
CAS No.:88346-64-9
Molecular Formula:C16H23N3O3S
Molecular Weight:337.443
Hs Code.:
DSSTox Substance ID:DTXSID90521532
Wikidata:Q82386058

Synonyms:88346-64-9;2-NITRO-N-[6-(1,3-THIAZOLIDIN-3-YL)HEXYL]BENZAMIDE;DTXSID90521532

Suppliers and Price of 2-Nitro-N-[6-(1,3-thiazolidin-3-YL)hexyl]benzamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Nitro-N-[6-(1,3-thiazolidin-3-YL)hexyl]benzamide

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:337.14601278
Heavy Atom Count:23
Complexity:389

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CSCN1CCCCCCNC(=O)C2=CC=CC=C2[N+](=O)[O-]

Technology Process of 2-Nitro-N-[6-(1,3-thiazolidin-3-YL)hexyl]benzamide

There total 2 articles about 2-Nitro-N-[6-(1,3-thiazolidin-3-YL)hexyl]benzamide 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: 99.0%

: 88346-63-8
3-(6-aminohexyl)-1,3-thiazolidine

: 610-14-0
2-nitrobenzyl chloride

: 88346-64-9
N-<6-(3-thiazolidyl)hexyl>-o-nitrobenzamide

Guidance literature:: With triethylamine; In benzene; for 5h; Ambient temperature;
DOI:10.1002/jhet.5570200525

Reference yield:

: 124-09-4
1,6-Hexanediamine

: 88346-64-9
N-<6-(3-thiazolidyl)hexyl>-o-nitrobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1) benzene, reflux, 2 h, 2) aq. methanol, reflux, 12 h

2: 99 percent / triethylamine / benzene / 5 h / Ambient temperature

With triethylamine; In benzene;
DOI:10.1002/jhet.5570200525