881099-32-7

Basic information

• Product Name: [(3S,5S)-3-(2-Methyl-allyl)-2-oxo-5-phenyl-morpholine-4-carbothioyl]-carbamic acid benzyl ester
• Synonyms: [(3S,5S)-3-(2-Methyl-allyl)-2-oxo-5-phenyl-morpholine-4-carbothioyl]-carbamic acid benzyl ester
• CAS NO: 881099-32-7
• Molecular Weight: 424.521
• Mol File: 881099-32-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(3S,5S)-3-(2-Methyl-allyl)-2-oxo-5-phenyl-morpholine-4-carbothioyl]-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(3S,5S)-3-(2-Methyl-allyl)-2-oxo-5-phenyl-morpholine-4-carbothioyl]-carbamic acid benzyl ester(881099-32-7)
• EPA Substance Registry System: [(3S,5S)-3-(2-Methyl-allyl)-2-oxo-5-phenyl-morpholine-4-carbothioyl]-carbamic acid benzyl ester(881099-32-7)

Safety Data

• Hazardous Substances Data: 881099-32-7(Hazardous Substances Data)

Upstream product

• 881099-31-6 (3S,5S)-3-(2-methylallyl)-5-phenyl-3,4,5,6-tetrahydro-1,4-oxazin-2-one 
• 63220-36-0 benzyloxycarbonyl isothiocyanate 
• 20989-17-7 (2S)-2-phenylglycinol 
• 881099-30-5 (S)-2-((S)-2-Hydroxy-1-phenyl-ethylamino)-4-methyl-pent-4-enoic acid ethyl ester 

Relevant articles and documents

New utilizations of optically active homoallylamines: Highly stereoselective synthesis of cyclic guanidine and thiourea

Halocyclizations of optically active homoallylguanidine and homoallylthiourea were examined. These reactions proceeded stereoselectively to give six membered cyclic guanidines and thiourea. High 1,3-asymmetric induction by the homoallylic substituents is