393109-24-5

Basic information

• Product Name: Propanoic acid, 2,2-dimethyl-, (2S)-2-hydroxy-4-(phenylmethoxy)butyl ester
• CAS NO: 393109-24-5
• Molecular Formula: C16H24O4
• Molecular Weight: 280.364
• Mol File: 393109-24-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 2,2-dimethyl-, (2S)-2-hydroxy-4-(phenylmethoxy)butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2,2-dimethyl-, (2S)-2-hydroxy-4-(phenylmethoxy)butyl ester(393109-24-5)
• EPA Substance Registry System: Propanoic acid, 2,2-dimethyl-, (2S)-2-hydroxy-4-(phenylmethoxy)butyl ester(393109-24-5)

Safety Data

• Hazardous Substances Data: 393109-24-5(Hazardous Substances Data)

Upstream product

• 71998-69-1 (S)-4-benzyloxy-1,2-butanediol 
• 3282-30-2 pivaloyl chloride 

Downstream Products

• 393109-25-6 2,2-Dimethyl-propionic acid (S)-4-benzyloxy-2-methanesulfonyloxy-butyl ester 
• 393109-23-4 (S)-((4-(benzyloxy)butan-2-yl)oxy)(tert-butyl)dimethylsilane 
• 500318-50-3 (R)-4-benzyloxy-1-(pivaloyl)oxy-2-butanol 
• 4799-69-3 (S)-(-)-1,3-butanediol 1-benzyl ether 

Relevant articles and documents

Acceleration of hetero-Michael reaction by symmetrical pentacyclic guanidines

Symmetrical pentacyclic guanidines 1a-c and 2 which contain the core skeleton of 13,14,15-isocrmbescidine 800, have been synthesized. In the presence of catalytic amounts of these guanidines 1, the reaction rate of the conjugate addition of pyrrolidine (9) to γ-crotonolactone (10) could be enhanced depending upon the size of the cavities and substituents on tetrahydropyran rings of 1 and 2.