432512-66-8

Basic information

• Product Name: N-(2-isopropylphenyl)-N'-(4-methoxybenzoyl)thiourea
• Synonyms: N-(2-isopropylphenyl)-N'-(4-methoxybenzoyl)thiourea;4-methoxy-N-{[2-(propan-2-yl)phenyl]carbamothioyl}benzamide;Benzamide, 4-methoxy-N-[[[2-(1-methylethyl)phenyl]amino]thioxomethyl]-
• CAS NO: 432512-66-8
• Molecular Formula: C18H20N2O2S
• Molecular Weight: 328.43
• Mol File: 432512-66-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-isopropylphenyl)-N'-(4-methoxybenzoyl)thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-isopropylphenyl)-N'-(4-methoxybenzoyl)thiourea(432512-66-8)
• EPA Substance Registry System: N-(2-isopropylphenyl)-N'-(4-methoxybenzoyl)thiourea(432512-66-8)

Safety Data

• Hazardous Substances Data: 432512-66-8(Hazardous Substances Data)

Upstream product

• 1147550-11-5 ammonium thiocyanate 
• 100-07-2 4-methoxy-benzoyl chloride 
• 643-28-7 2-isopropylaniline 

Relevant articles and documents

N-Heterocyclic Carbene-Catalyzed Atroposelective Annulation for Access to Thiazine Derivatives with C?N Axial Chirality

A catalytic atroposelective cycloaddition reaction between thioureas and ynals is developed. This reaction features the first NHC-catalyzed addition of thioureas to acetylenic acylazolium intermediates to eventually set up C?N axial chirality with excellent optical purities. The obtained axially chiral thiazine derivative products bear multiple functional groups and are feasible for further transformations.