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Supidimide

Base Information
  • Chemical Name:Supidimide
  • CAS No.:49785-74-2
  • Molecular Formula:C12H12N2O4S
  • Molecular Weight:280.304
  • Hs Code.:
  • European Community (EC) Number:256-490-3
  • UNII:L2GWR3US1G
  • DSSTox Substance ID:DTXSID40866142
  • Nikkaji Number:J10.372A
  • Wikidata:Q27282622
  • NCI Thesaurus Code:C74382
  • ChEMBL ID:CHEMBL72115
Supidimide

Synonyms:CG 3033;supidimide

Suppliers and Price of Supidimide
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
  • American Custom Chemicals Corporation
  • SUPIDIMIDE 95.00%
  • 5MG
  • $ 497.20
Total 5 raw suppliers
Chemical Property of Supidimide
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:95.42000 
  • Density:1.512g/cm3 
  • LogP:1.40430 
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:280.05177804
  • Heavy Atom Count:19
  • Complexity:510
Purity/Quality:

99% *data from raw suppliers

SUPIDIMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(C(=O)NC1)N2C(=O)C3=CC=CC=C3S2(=O)=O
Technology Process of Supidimide

There total 2 articles about Supidimide 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:
Guidance literature:
In N,N-dimethyl-formamide; at 140 ℃; for 0.166667h;

Reference yield:

Guidance literature:
α-(o-Sulfobenzoesaeureimido)-γ-cyano-buttersaeure-ethylester, 1. H2(Ni), 2. Cyclisierung;
Guidance literature:
With potassium hydroxide; In 1,4-dioxane; at 20 ℃; for 1h;
upstream raw materials:

3-bromo-2-piperidinone

Downstream raw materials:

N-(2-oxopiperidin-3-yl)-2-(aminosulfonyl)-benzoic acid

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