1432059-19-2

Basic information

• Product Name: C₂₂H₂₀Cl₂N₂O₃
• Synonyms: C₂₂H₂₀Cl₂N₂O₃
• CAS NO: 1432059-19-2
• Molecular Weight: 431.318
• Mol File: 1432059-19-2.mol

Chemical Properties

• CAS DataBase Reference: C₂₂H₂₀Cl₂N₂O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₂H₂₀Cl₂N₂O₃(1432059-19-2)
• EPA Substance Registry System: C₂₂H₂₀Cl₂N₂O₃(1432059-19-2)

Safety Data

• Hazardous Substances Data: 1432059-19-2(Hazardous Substances Data)

Upstream product

• 945736-71-0 (E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione 
• 68014-21-1 triphenyl(t-butoxycarbonylimino)phosphorane 
• 149946-25-8 (E)-4-(3-bromoprop-1-en-1-yl)-1,2-dichlorobenzene 
• 148775-22-8 3-(3,4-dichlorophenyl)-prop-2-en-1-ol 
• 40950-94-5 ethyl (E)-3-(3,4-dichloro-phenyl)-2-propenoate 
• 6287-38-3 3,4-dichlorobenzaldehyde 

Downstream Products

• 1432059-82-9 tert-butyl (E)-(3-cyano-1-(3-(3,4-dichlorophenyl)allyl)-2-oxoindolin-3-yl)carbamate 
• 1432059-42-1 (R,E)-tert-butyl {3-cyano-1-[3-(3,4-dichlorophenyl)allyl]-2-oxoindolin-3-yl}carbamate 
• 1432059-83-0 (S,E)-3-amino-1-(3-(3,4-dichlorophenyl)allyl)-2-oxoindoline-3-carbonitrile 

Relevant articles and documents

Organocatalytic asymmetric cyanation of isatin derived N-Boc ketoimines

We report the first catalytic asymmetric cyanation of N-Boc ketoimines, which enables highly enantioselective synthesis of oxindole based α-amino nitriles. An unprecedented tandem aza-Wittig/Strecker reaction is also developed, emerging as a promising strategy for the catalytic asymmetric cyanation of ketoimines formed in situ from achiral ketones.