1240507-88-3

Basic information

• Product Name: C₃₆H₅₅N₅O₁₁S
• Synonyms: C₃₆H₅₅N₅O₁₁S
• CAS NO: 1240507-88-3
• Molecular Weight: 765.926
• Mol File: 1240507-88-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₃₆H₅₅N₅O₁₁S(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₆H₅₅N₅O₁₁S(1240507-88-3)
• EPA Substance Registry System: C₃₆H₅₅N₅O₁₁S(1240507-88-3)

Safety Data

• Hazardous Substances Data: 1240507-88-3(Hazardous Substances Data)

Upstream product

• 1494545-59-3 C₃₂H₅₄N₄O₇Si 
• 1494545-57-1 C₂₆H₄₃N₃O₆Si 
• 1494545-55-9 C₂₀H₃₂N₂O₅Si 
• 1240507-79-2 (S)-HA-Pro-OH 
• 1494545-35-5 C₂₄H₄₈N₄O₅Si 
• 1494545-83-3 C₁₈H₃₇N₃O₄Si 
• 1494545-81-1 C₁₂H₂₆N₂O₃Si 
• 1240507-83-8 (S)-HA-Pro-OBn 
• 1494545-40-2 N-[2-(R)-(tert-butyldimethylsiloxy)pent-4-enoyl]-L-proline benzyl ester 
• 1494545-45-7 (R)-2-(tert-butyldimethylsilyloxy)pent-4-enoic acid methyl ester 
• 1494545-48-0 (R)-2-((tert-butyldimethylsilyl)oxy)pent-4-enoic acid 
• 1240507-87-2 C₃₂H₅₃N₅O₉ 
• 1240507-78-1 C₃₂H₅₅N₅O₁₀ 
• 1494545-61-7 C₄₃H₈₁N₅O₁₀Si₂ 

Downstream Products

• 76689-14-0 destruxin E 

Relevant articles and documents

Scalable solution-phase synthesis of the biologically active cyclodepsipeptide destruxin E, a potent negative regulator of osteoclast morphology

The scalable solution-phase synthesis of the cyclodepsipeptide destruxin E (1) has been achieved. Diastereoselective dihydroxylation of the terminal alkene in a 2-alkoxy-4-pentenoic amide, 7, was successfully accomplished utilizing (DHQD)2PHAL

Synthesis, structure determination, and biological evaluation of destruxin e

The total synthesis of destruxin E (1) has been achieved for the first time, and the stereochemistry of its chiral center at the epoxide has been determined to be (S). The cyclization precursor 3a was synthesized by solid-phase peptide synthesis. Macrolac