1448686-69-8

Basic information

• Product Name: 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
• Synonyms: 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
• CAS NO: 1448686-69-8
• Molecular Weight: 1323.92
• Mol File: 1448686-69-8.mol

Chemical Properties

• CAS DataBase Reference: 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(CAS DataBase Reference)
• NIST Chemistry Reference: 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(1448686-69-8)
• EPA Substance Registry System: 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(1448686-69-8)

Safety Data

• Hazardous Substances Data: 1448686-69-8(Hazardous Substances Data)

Upstream product

• 1448686-65-4 11(S)-levulinoyloxyhexadecanoic acid 
• 1448686-64-3 11(S)-levulinoyloxy-1-hexadecanol 
• 1448686-63-2 11(S)-levulinoyloxy-1-phenylmethoxylhexadecane 
• 1448686-62-1 allyl 2-O-2(S)-methylbutyryl-4-O-tert-butyldimethylsilyl-α-L-rhamnopyranoside 
• 929296-51-5 (S)-1-benzyloxy-11-hexadecanol 
• 1240486-90-1 allyl 2-O-2(S)-methylbutyryl-3-O-p-methoxybenzyl-4-O-tert-butyldimethylsilyl-α-L-rhamnopyranoside 
• 545-06-2 trichloroacetonitrile 
• 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 
• 1448686-67-6 allyl 2-O-2(S)-methylbutyryl-3-O-(11(S)-levulinoyloxyhexadecanoyl)-α-L-rhamnopyranoside 
• 1448686-66-5 allyl 2-O-2(S)-methylbutyryl-3-O-(11(S)-levulinoyloxyhexadecanoyl)-4-O-tert-butyldimethylsilyl-α-L-rhamnopyranoside 

Downstream Products

• 1448686-71-2 C₁₀₆H₁₆₂O₂₇ 

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.