1574776-16-1

Basic information

• Product Name: C₆₁H₈₈N₁₀O₁₉
• Synonyms: C₆₁H₈₈N₁₀O₁₉
• CAS NO: 1574776-16-1
• Molecular Weight: 1265.43
• Mol File: 1574776-16-1.mol

Chemical Properties

• CAS DataBase Reference: C₆₁H₈₈N₁₀O₁₉(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₁H₈₈N₁₀O₁₉(1574776-16-1)
• EPA Substance Registry System: C₆₁H₈₈N₁₀O₁₉(1574776-16-1)

Safety Data

• Hazardous Substances Data: 1574776-16-1(Hazardous Substances Data)

Upstream product

• 1515605-74-9 (S)-[5-azido-1-(triphenylmethoxy)-2-pentyloxy]triisopropylsilane 
• 1515605-73-8 4(S)-triisopropylsilyloxy-5-triphenylmethoxy-1-pentanol 
• 1515605-70-5 (S)-triisopropyl[1-(triphenylmethoxy)pent-4-en-2-yloxy]silane 
• 1515605-87-4 C₃₁H₄₅N₅O₉*ClH 
• 1515605-47-6 N-Cbz-D-Ser(N-Boc-N-Me-Val)-OH 
• 1515605-81-8 C₄₃H₅₇N₅O₁₃S 
• 1515605-52-3 C₁₄H₂₉N₃O₂Si 
• 1515605-49-8 C₁₄H₂₉NOSi 
• 1515606-36-6 C₄₀H₅₂O₅SSi 
• 1515605-46-5 2-propenyl 2-(2-isocyano-N-methylacetamido)acetate 
• 170277-82-4 (2S)-1-triphenylmethoxy-4-pentene-2-ol 
• 45170-31-8 Boc-N-Me-Val-OH 
• 78700-33-1 Z-D-Ser-OTce 
• 1515605-59-0 N-formyl-Gly-Sar allyl ester 

Relevant articles and documents

Total synthesis of sandramycin and its analogues via a multicomponent assemblage

The total synthesis of sandramycin has been accomplished by using a Staudinger/aza-Wittig/diastereoselective Ugi three-component reaction sequence as a key step to obtain a linear pentadepsipeptide. Subsequent [5 + 5] coupling of the penptapeptide, macrolactamization, and introduction of the quinaldin chromophores afforded sandramycin. Dihydroxy and diacetoxy analogues were also prepared, and the cytotoxic activity of these analogues against a range of human cancer cell lines was evaluated.