1313506-39-6

Basic information

• Product Name: 1-(2-benzyl-1,3-dioxoisoindolin-5-yl)-3-((R)-1-phenyl-ethyl)thiourea
• CAS NO: 1313506-39-6
• Molecular Weight: 415.516
• Mol File: 1313506-39-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2-benzyl-1,3-dioxoisoindolin-5-yl)-3-((R)-1-phenyl-ethyl)thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-benzyl-1,3-dioxoisoindolin-5-yl)-3-((R)-1-phenyl-ethyl)thiourea(1313506-39-6)
• EPA Substance Registry System: 1-(2-benzyl-1,3-dioxoisoindolin-5-yl)-3-((R)-1-phenyl-ethyl)thiourea(1313506-39-6)

Safety Data

• Hazardous Substances Data: 1313506-39-6(Hazardous Substances Data)

Upstream product

• 83051-28-9 5-amino-2-benzyl-2,3-dihydro-1H-isoindole-1,3-dione 
• 136918-14-4 phthalimide 
• 1313506-40-9 2-benzyl-5-isothiocyanatoisoindoline-1,3-dione 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 89-40-7 4-nitrophthalimide 
• 60283-84-3 2-benzyl-5-nitroisoindoline-1,3-dione 

Relevant articles and documents

Colorimetric detection of achiral anions and chiral carboxylates by a chiral thiourea-phthalimide dyad

The chiral chemosensor 1, based on a thiourea-activated phthalimide, is available by four reaction steps from 4-nitrophthalimide. 1 detects fluoride, chloride, acetate, and dihydrogen phosphate anions by changes in UV-vis absorption. Fluoride in excess induces deprotonation whereas the other anions show only complex formation in the ground state. 1H-NMR studies confirm the formation of these H-bonded complexes and the fluoride-induced receptor deprotonation in the recognition process. Moderate chiral recognition was observed for sodium d/l-lactate with Kass(d)/Kass(l) = 1.93.