102936-73-2

Basic information

• Product Name: 3-cyclohexylthiazolidine-2,4-dione
• Synonyms: 3-cyclohexylthiazolidine-2,4-dione
• CAS NO: 102936-73-2
• Molecular Weight: 199.274
• Mol File: 102936-73-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-cyclohexylthiazolidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-cyclohexylthiazolidine-2,4-dione(102936-73-2)
• EPA Substance Registry System: 3-cyclohexylthiazolidine-2,4-dione(102936-73-2)

Safety Data

• Hazardous Substances Data: 102936-73-2(Hazardous Substances Data)

Upstream product

• 108-85-0 1-bromocyclohexane 
• 2295-31-0 thiazoline-2,4-dione 
• 39131-10-7 1,3-thiazolidine-2,4-dione potassium salt 
• 722-03-2 N-cyclohexyl-N'-phenylthiourea 
• 102936-66-3 3-Cyclohexyl-2-[(Z)-phenylimino]-thiazolidin-4-one 
• 114710-78-0 2-[(Z)-Allylimino]-3-cyclohexyl-thiazolidin-4-one 
• 722-03-2 N¹-phenyl-N²-cyclohexylthiourea 
• 77563-68-9 N¹-allyl-N²-cyclohexylthiourea 
• 108-91-8 cyclohexylamine 

Downstream Products

• 1149337-56-3 (Z)-3-cyclohexyl-5-{[5-(3-nitrophenyl)furan-2-yl]methylene}thiazolidine-2,4-dione 

Relevant articles and documents

Dual inhibitors of the dengue and West Nile virus NS2B-NS3 proteases: Synthesis, biological evaluation and docking studies of novel peptide-hybrids

Dengue virus (DENV) and West Nile virus (WNV) are mosquito-borne arboviruses responsible for causing acute systemic diseases and severe health conditions in humans. The discovery of therapies capable to prevent infections or treat infected individuals rem

Influence of Substituents on the Synthesis of Thiazolidinones

The influence of substituents (subunits) in the synthesis of thiazolidinones by the reaction of unsymmetrical thioureas with monochloroacetic acid in ethanol has been rationalised by the characterisation of the hydrolysis products of the resulting thiazolidinones.The formation of thiol from thiourea, which is the key intermediate in thiazolidinone synthesis, invariably involves the -NH- group adjacent to more electron withdrawing subunits.