130984-56-4

Basic information

• Product Name: C₃₀H₃₀N₂O₂S
• Synonyms: C₃₀H₃₀N₂O₂S
• CAS NO: 130984-56-4
• Molecular Weight: 482.646
• Mol File: 130984-56-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₃₀H₃₀N₂O₂S(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₃₀N₂O₂S(130984-56-4)
• EPA Substance Registry System: C₃₀H₃₀N₂O₂S(130984-56-4)

Safety Data

• Hazardous Substances Data: 130984-56-4(Hazardous Substances Data)

Upstream product

• 123054-12-6 (2S)-N,N-dibenzylphenylalaninal 
• 4104-47-6 N-sulfinyl-p-toluenesulfonamide 

Downstream Products

• 130984-72-4 N-((1R,2S)-2-Dibenzylamino-1,3-diphenyl-propyl)-4-methyl-benzenesulfonamide 
• 130984-72-4 N-((1S,2S)-2-Dibenzylamino-1,3-diphenyl-propyl)-4-methyl-benzenesulfonamide 
• 1065519-42-7 (+)-(2R,1'S)-1-tosyl-2-[1'-(dibenzylamino)-2'-phenylethyl]aziridine 
• 1126144-77-1 (2S,3S)-1-chloro-N₃,N₃-dibenzyl-4-phenyl-N₂-tosylbutane-2,3-diamine 
• 130984-96-2 (2S,3R)-1-Phenyl-butane-2,3-diamine 
• 130984-94-0 (4S,5R)-4-Benzyl-5-methyl-1-(toluene-4-sulfonyl)-imidazolidin-2-one 
• 130984-93-9 N-((1R,2S)-2-Amino-1-methyl-3-phenyl-propyl)-4-methyl-benzenesulfonamide 
• 130984-95-1 (2S,3R)-N²,N²-Dibenzyl-1-phenyl-butane-2,3-diamine 
• 130984-71-3 N-[(R)-1-((S)-1-Dibenzylamino-2-phenyl-ethyl)-pentyl]-4-methyl-benzenesulfonamide 
• 130984-70-2 N-[(S)-1-((S)-1-Dibenzylamino-2-phenyl-ethyl)-pentyl]-4-methyl-benzenesulfonamide 
• 130984-74-6 N-[(R)-1-((S)-1-Dibenzylamino-2-phenyl-ethyl)-but-3-enyl]-4-methyl-benzenesulfonamide 
• 130984-74-6 N-[(S)-1-((S)-1-Dibenzylamino-2-phenyl-ethyl)-but-3-enyl]-4-methyl-benzenesulfonamide 
• 130984-73-5 N-[(R)-1-((S)-1-Dibenzylamino-2-phenyl-ethyl)-allyl]-4-methyl-benzenesulfonamide 
• 130984-73-5 N-[(S)-1-((S)-1-Dibenzylamino-2-phenyl-ethyl)-allyl]-4-methyl-benzenesulfonamide 

Relevant articles and documents

Addition reactions of chloro- Or iodomethyllithium to imines. Synthesis of enantiopure aziridines and β-chloroamines

We report a novel, simple, and efficient synthesis of aziridines and l-chloroalkan-2-amines by the reaction of imines derived from various aldehydes and p-toluenesulfonamide or benzenesulfonamide with iodoor chloromethyllithium, respectively. Both halogenated anions were generated in situ by treatment of diiodo- or chloroiodomethane with methyllithium at -78 or 0 °C. The reaction of in situ generated iodoor chloromethyllithium could also be performed from chiral 2-aminoaldimines to yield enantiopure aziridines or (2S,3S)-2,3-diamino- l-chloroalkanes with high stereoselectivity.

Stereoselektive Synthese von vicinalen Diaminen

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