77563-68-9

Basic information

• Product Name: 1-allyl-3-cyclohexylthiourea
• Synonyms: 1-allyl-3-cyclohexylthiourea
• CAS NO: 77563-68-9
• Molecular Weight: 198.332
• Mol File: 77563-68-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-allyl-3-cyclohexylthiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-allyl-3-cyclohexylthiourea(77563-68-9)
• EPA Substance Registry System: 1-allyl-3-cyclohexylthiourea(77563-68-9)

Safety Data

• Hazardous Substances Data: 77563-68-9(Hazardous Substances Data)

Upstream product

• 108-91-8 cyclohexylamine 
• 57-06-7 N-allyl isothiocyanate 
• 931-53-3 Cyclohexyl isocyanide 
• 107-11-9 1-amino-2-propene 

Downstream Products

• 102936-73-2 3-cyclohexylthiazolidine-2,4-dione 
• 114710-78-0 2-[(Z)-Allylimino]-3-cyclohexyl-thiazolidin-4-one 
• 62490-37-3 allyl-cyclohexyl-carbodiimide 

Relevant articles and documents

Three-component reaction between isocyanides, aliphatic amines and elemental sulfur: Preparation of thioureas under mild conditions with complete atom economy

The reaction of isocyanides with aliphatic amines in the presence of elemental sulfur was found to proceed efficiently at, or near, room temperature to produce thioureas in excellent yields and with complete atom economy.

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.