409305-55-1

Basic information

• Product Name: 2-Oxazolidinone, 3-[[(1S)-1-phenyl-3-butenyl]amino]-4-(phenylmethyl)-, (4S)-
• CAS NO: 409305-55-1
• Molecular Formula: C20H22N2O2
• Molecular Weight: 322.407
• Mol File: 409305-55-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-[[(1S)-1-phenyl-3-butenyl]amino]-4-(phenylmethyl)-, (4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-[[(1S)-1-phenyl-3-butenyl]amino]-4-(phenylmethyl)-, (4S)-(409305-55-1)
• EPA Substance Registry System: 2-Oxazolidinone, 3-[[(1S)-1-phenyl-3-butenyl]amino]-4-(phenylmethyl)-, (4S)-(409305-55-1)

Safety Data

• Hazardous Substances Data: 409305-55-1(Hazardous Substances Data)

Upstream product

• 1112-66-9 tetraallylsilane 
• 299216-18-5 (S)-3-(benzylidene)amino-4-phenylmethyl-2-oxazolidinone 
• 106-95-6 allyl bromide 
• 299216-13-0 (S)-3-amino-4-benzyl-1,3-oxazolan-2-one 
• 100-52-7 benzaldehyde 
• 106948-24-7 (allyl)(diisopropylamino)dimethylsilane 

Downstream Products

• 669081-18-9 N-(4-benzyl-2-oxo-oxazolidin-3-yl)-N-(1-phenyl-but-3-enyl)-benzamide 

Relevant articles and documents

Tin powder-promoted diastereoselective allylation of chiral acylhydrazones

An efficient method for the allylation of chiral acylhydrazones derived from aldehydes has been developed to give the corresponding allylic hydrazides in good yields and diastereoselectivities. The method uses a combination of tin powder and allylic bromide as allylation system, which avoids the use of toxic allylic stannanes while retaining their merits.

Asymmetric allylsilane additions to enantiopure N-acylhydrazones with dual activation by fluoride and In(OTF)3

A mild, convenient, and stereoselective addition of allylsilanes to enantiopure N-acylhydrazones occurs at room temperature upon complementary activation of both the allylsilane and the hydrazone (see scheme; OTf = trifluoromethanesulfonate). The reaction