1448686-63-2

Basic information

• Product Name: 11(S)-levulinoyloxy-1-phenylmethoxylhexadecane
• Synonyms: 11(S)-levulinoyloxy-1-phenylmethoxylhexadecane
• CAS NO: 1448686-63-2
• Molecular Weight: 446.671
• Mol File: 1448686-63-2.mol

Chemical Properties

• CAS DataBase Reference: 11(S)-levulinoyloxy-1-phenylmethoxylhexadecane(CAS DataBase Reference)
• NIST Chemistry Reference: 11(S)-levulinoyloxy-1-phenylmethoxylhexadecane(1448686-63-2)
• EPA Substance Registry System: 11(S)-levulinoyloxy-1-phenylmethoxylhexadecane(1448686-63-2)

Safety Data

• Hazardous Substances Data: 1448686-63-2(Hazardous Substances Data)

Upstream product

• 929296-51-5 (S)-1-benzyloxy-11-hexadecanol 

Downstream Products

• 1448686-68-7 allyl 2-O-trans-cinnamoyl-3-O-p-methoxybenzyl-4-O-n-dodecanoyl-α-L-rhamnopyranosyl-(1→4)-2-O-2(S)-methylbutyryl-3-O-(11(S)-levulinoyloxyhexadecanoyl)-α-L-rhamnopyranoside 
• 1448686-69-8 2-O-trans-cinnamoyl-3-O-p-methoxybenzyl-4-O-n-dodecanoyl-α-L-rhamnopyranosyl-(1→4)-2-O-2(S)-methylbutyryl-3-O-(11(S)-levulinoyloxyhexadecanoyl)-α-L-rhamnopyranosyl trichloroacetimidate 

Relevant articles and documents

First total synthesis of the proposed structure of batatin VI

The first total synthesis of batatin VI, an architecturally novel resin glycoside dimer, has been achieved via a convergent [5 + 3] glycosidic coupling approach. An improved protocol for the construction of the key 18-membered macrolactone core using a Keck macrolactonization method was introduced. However, the synthesized compound was not identical to the natural batatin VI.