259675-59-7

Basic information

• Product Name: 4-hydroxy-undecanoic acid benzylamide
• CAS NO: 259675-59-7
• Molecular Weight: 291.434
• Mol File: 259675-59-7.mol

Chemical Properties

• CAS DataBase Reference: 4-hydroxy-undecanoic acid benzylamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-undecanoic acid benzylamide(259675-59-7)
• EPA Substance Registry System: 4-hydroxy-undecanoic acid benzylamide(259675-59-7)

Safety Data

• Hazardous Substances Data: 259675-59-7(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 104-67-6 5-heptyldihydro-2(3H)-furanone 

Downstream Products

• 259675-64-4 Succinic acid mono-[(S)-1-(2-benzylcarbamoyl-ethyl)-octyl] ester 
• 1233882-47-7 C₂₀H₃₁NO₃ 
• 945595-25-5 C₂₀H₃₁NO₃ 
• 1163138-30-4 (S)-N-benzyl-4-(4-nitrobenzoyl)oxyundecanamide 
• 74568-05-1 (4S)-4-heptyl-γ-butanolide 

Relevant articles and documents

Synthesis of (S)-γ- lactones with a combination of lipase-catalyzed resolution and mitsunobu reaction

Six kinds of (S) - lactones [e.g., (S) - decalactone, (S) - undecalactone, and (S) - jasmolactone] were synthesized with 71-88% yields and 97% optical purities by combining lipase-catalyzed resolution with the Mitsunobu reaction. Copyright Taylor & Francis Group, LLC.

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