446064-67-1

Basic information

• Product Name: C₆₈H₉₄Cl₃N₉O₁₆Si
• CAS NO: 446064-67-1
• Molecular Weight: 1427.99
• Mol File: 446064-67-1.mol

Chemical Properties

• CAS DataBase Reference: C₆₈H₉₄Cl₃N₉O₁₆Si(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₈H₉₄Cl₃N₉O₁₆Si(446064-67-1)
• EPA Substance Registry System: C₆₈H₉₄Cl₃N₉O₁₆Si(446064-67-1)

Safety Data

• Hazardous Substances Data: 446064-67-1(Hazardous Substances Data)

Upstream product

• 446064-66-0 (E)-(S)-4-((2R,3S)-2-Amino-3-methyl-pentanoylamino)-5-(4-triisopropylsilanyloxy-phenyl)-pent-2-enoic acid allyl ester 
• 446064-63-7 C₅₈H₆₂Cl₃N₈O₁₁P 
• 104127-76-6 allyl (triphenylphosphoranylidene)acetate 
• 51219-19-3 N^α-tert-butoxycarbonyl-N^δ,N^ω-di-benzyloxycarbonyl-L-arginine 
• 73259-80-0 N²-(2,2,2-trichloroethoxycarbonyl)-L-2,3-diaminopropanoic acid 
• 151133-13-0 [(S)-1-Formyl-2-(4-triisopropylsilanyloxy-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 446064-61-5 (S)-1-[(S)-3-tert-Butoxycarbonylamino-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionyl]-pyrrolidine-2-carboxylic acid 
• 446064-64-8 (E)-(S)-4-tert-Butoxycarbonylamino-5-(4-triisopropylsilanyloxy-phenyl)-pent-2-enoic acid allyl ester 
• 446064-62-6 N^α-Boc-N^δ,N^ε-Z₂-Arg-C(PPH3)CN 
• 446064-65-9 (E)-(S)-4-((2R,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoylamino)-5-(4-triisopropylsilanyloxy-phenyl)-pent-2-enoic acid allyl ester 
• 477331-81-0 (S)-1-[(S)-3-tert-Butoxycarbonylamino-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionyl]-pyrrolidine-2-carboxylic acid benzyl ester 
• 735327-63-6 (S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-(triisopropylsilyloxy)phenyl)propanoate 
• 446064-60-4 3-tert-butoxycarbonylamino-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid 
• 78221-36-0 Teoc-aspargine 

Downstream Products

• 446064-72-8 C₆₅H₉₀Cl₃N₉O₁₆Si 

Relevant articles and documents

Total synthesis of cyclotheonamides E2 and E3: Application of cyano ylide methodology

A total synthesis of cyclotheonamides E2 and E3 is reported. A key step in the synthesis involves the formation of the α-keto amide linkage by application of the cyano ylide activation of a carboxyl group as developed in our earlier syntheses of cyclic peptides in the family of protease inhibitors.