147168-90-9

Basic information

• Product Name: (1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane
• Synonyms: (1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane
• CAS NO: 147168-90-9
• Molecular Weight: 197.301
• Mol File: 147168-90-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane(147168-90-9)
• EPA Substance Registry System: (1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane(147168-90-9)

Safety Data

• Hazardous Substances Data: 147168-90-9(Hazardous Substances Data)

Upstream product

• 147253-91-6 N-<(2R,3R)-3-hydroxy-2-methyl-3-phenylpropionyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 
• 147168-92-1 N-<(2S,3S)-3-hydroxy-2-methyl-3-phenylpropionyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 

Downstream Products

• 167259-98-5 N-<(R)-(E)-3-Hydroxy-5-phenyl-4-pentenoyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 
• 147168-92-1 N-<(2S,3S)-3-hydroxy-2-methyl-3-phenylpropionyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 
• 147253-91-6 N-<(2R,3R)-3-hydroxy-2-methyl-3-phenylpropionyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 
• 167260-00-6 N-<(R)-(E)-3-Hydroxy-5-(phenylthio)-4-pentenoyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 
• 167357-25-7 N-<(S)-(E)-3-Hydroxy-5-(phenylthio)-4-pentenoyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 
• 167357-22-4 N-<(S)-3-Hydroxy-3-phenylpropionyl>-(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.0^1,5>decane 

Relevant articles and documents

Asymmetric aldol reactions: A novel model for switching between chelation- and non-chelation-controlled aldol reactions

A new camphor-based N-propionyloxazolidinethione provides remarkable levels of asymmetric induction for both chelation- and non-chelation-controlled aldol processes. While the aldol condensation of the derived di-n-butylboryl enolate with various aldehyde