259675-58-6

Basic information

• Product Name: 4-hydroxy-decanoic acid benzylamide
• Synonyms: 4-hydroxy-decanoic acid benzylamide
• CAS NO: 259675-58-6
• Molecular Weight: 277.407
• Mol File: 259675-58-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-hydroxy-decanoic acid benzylamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-decanoic acid benzylamide(259675-58-6)
• EPA Substance Registry System: 4-hydroxy-decanoic acid benzylamide(259675-58-6)

Safety Data

• Hazardous Substances Data: 259675-58-6(Hazardous Substances Data)

Upstream product

• 706-14-9 5-hexyldihydro-2(3H)-furanone 
• 100-46-9 benzylamine 
• 3287-99-8 benzylamine hydrochloride 

Downstream Products

• 1233882-46-6 C₁₉H₂₉NO₃ 
• 945595-24-4 C₁₉H₂₉NO₃ 
• 107797-26-2 (R)-5-Hexyl-dihydro-furan-2-one 
• 107797-27-3 (-)-(S)-γ-Decalactone 
• 1163138-29-1 (S)-N-benzyl-4-(4-nitrobenzoyl)oxydecanamide 
• 259675-63-3 Succinic acid mono-[(S)-1-(2-benzylcarbamoyl-ethyl)-heptyl] ester 

Relevant articles and documents

A mild method for ring-opening aminolysis of lactones

A mild and general method for lactone aminolysis is reported. Sodium 2-ethylhexanoate (NaEH) is found to serve both as a base and a catalyst in aminolysis of a variety of lactones by benzylamine hydrochloride. The nearly neutral pH conditions make this method applicable to many acid/base sensitive substrates.

Facile synthesis of optically active γ-lactones via lipase-catalyzed reaction of 4-substituted 4-hydroxybutyramides

Lipase-catalyzed transesterification of racemic 4-substituted 4- hydroxybutyramides with succinic anhydride proceeded enantioselectively to afford (S)-succinic acid monoester and unreacted (R)-4-hydroxybutyramide derivative, which were separated easily by