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Sulindac

Base Information
  • Chemical Name:Sulindac
  • CAS No.:9000-14-0
  • Deprecated CAS:49627-22-7
  • Molecular Formula:
  • Molecular Weight:0
  • Hs Code.:
  • European Community (EC) Number:250-893-8,232-527-9,253-819-2
  • NSC Number:757344
  • UNII:184SNS8VUH
  • DSSTox Substance ID:DTXSID4023624
  • Nikkaji Number:J3.501G
  • Wikipedia:Sulindac
  • Wikidata:Q963093
  • NCI Thesaurus Code:C850
  • RXCUI:10237
  • Pharos Ligand ID:CLRLMAWF3NSM
  • Metabolomics Workbench ID:42934
  • ChEMBL ID:CHEMBL15770
Sulindac

Synonyms:Aclin;Apo Sulin;Apo-Sulin;Arthrobid;Arthrocine;Chibret;Clinoril;Copal;Kenalin;Klinoril;MK 231;MK-231;MK231;Novo Sundac;Novo-Sundac;Nu Sulindac;Nu-Sulindac;Sulindac;Sulindal

Suppliers and Price of Sulindac
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 10 raw suppliers
Chemical Property of Sulindac
Chemical Property:
  • PSA:0.00000 
  • LogP:0.00000 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:356.08824374
  • Heavy Atom Count:25
  • Complexity:616
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Chemical Classes:UVCB
  • Drug Classes:Nonsteroidal Antiinflammatory Drugs
  • Canonical SMILES:CC1=C(C2=C(C1=CC3=CC=C(C=C3)S(=O)C)C=CC(=C2)F)CC(=O)O
  • Isomeric SMILES:CC\1=C(C2=C(/C1=C\C3=CC=C(C=C3)S(=O)C)C=CC(=C2)F)CC(=O)O
  • Recent ClinicalTrials:The Prevention of Progression to Pancreatic Cancer Trial (The 3P-C Trial)
  • Recent EU Clinical Trials:The intestinal disposition of sulindac in healthy volunteers
  • Recent NIPH Clinical Trials:A randomized, double-blind, placebo-controlled trial for evaluating of suppressive effect of sulindac on branch duct type Intraductal papillary mucinous neoplasms
  • Description Copal is the general name for fossil and other hard resins found in almost all tropical countries. All are distinguished by their yellowish to yellowish-brown color and their solubility in chloral hydrate, alcohol, linseed oil, and turpentine. Their main use is in the manufacture of lacquers, varnishes, coatings, and adhesives.
  • Uses In varnishes and cements; as substitute for amber; manufacture of oil cloths and linoleum. In dentistry, for modeling Compounds and cavity varnishes.
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