611182-70-8

Basic information

• Product Name: TIPSO-D-Hpla(TIPS)-D-Leu-L-Choi(TIPS)-L-Arg(δ,ω'-di-Cbz)-OMe
• Synonyms: TIPSO-D-Hpla(TIPS)-D-Leu-L-Choi(TIPS)-L-Arg(δ,ω'-di-Cbz)-OMe
• CAS NO: 611182-70-8
• Molecular Weight: 1370.06
• Mol File: 611182-70-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: TIPSO-D-Hpla(TIPS)-D-Leu-L-Choi(TIPS)-L-Arg(δ,ω'-di-Cbz)-OMe(CAS DataBase Reference)
• NIST Chemistry Reference: TIPSO-D-Hpla(TIPS)-D-Leu-L-Choi(TIPS)-L-Arg(δ,ω'-di-Cbz)-OMe(611182-70-8)
• EPA Substance Registry System: TIPSO-D-Hpla(TIPS)-D-Leu-L-Choi(TIPS)-L-Arg(δ,ω'-di-Cbz)-OMe(611182-70-8)

Safety Data

• Hazardous Substances Data: 611182-70-8(Hazardous Substances Data)

Upstream product

• 80522-42-5 triisopropylsilyl trifluoromethanesulfonate 
• 24277-39-2 N-tert-butoxycarbonyl glutamic acid tert-butyl ester 
• 50299-15-5 methyl (S)-allylglycinate 
• 90194-99-3 tert-butyl (S)-2-<(tert-butyloxycarbonyl)amino>-5-hydroxypentanoate 
• 611182-68-4 Boc-L-Choi(TIPS)-L-Arg(δ,ω'-di-Cbz)-OMe 
• 611182-67-3 C₃₇H₄₉N₅O₁₀ 
• 611182-65-1 HO-D-Hpla(TIPS)-D-Leu-O-t-Bu 
• 139033-70-8 L-Arg(δ,ω'-di-Cbz)-OMe 
• 611182-62-8 N-(diphenylmethylene)-L-glutamic acid 1-(1,1-dimethylethyl) 5-benzyl ester 
• 373368-60-6 (2S,3aS,6R,7aS)-1-tert-Butoxycarbonyl-6-hydroxy-octahydroindole-2-carboxylic acid 
• 313952-04-4 methyl (2S,3aS,6R,7aS)-1-tert-butoxycarbonyl-6-hydroxy-octahydroindole-2-carboxylate 
• 162007-07-0 methyl (2S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate 
• 119244-19-8 tert-butyl (S)-2-[(diphenylmethylene)amino]pent-4-enoate 
• 611182-66-2 (R)-4-Methyl-2-[(R)-2-triisopropylsilanyloxy-3-(4-triisopropylsilanyloxy-phenyl)-propionylamino]-pentanoic acid 

Downstream Products

• 611182-71-9 TIPSO-D-Hpla(TIPS)-D-Leu-L-Choi(TIPS)-L-Argol(δ,ω'-di-Cbz) 

Relevant articles and documents

Enantioselective syntheses of aeruginosin 298-A and its analogues using a catalytic asymmetric phase-transfer reaction and epoxidation

We developed a versatile synthetic process for aeruginosin 298-A as well as several attractive analogues, in which all stereocenters were controlled by a catalytic asymmetric phase-transfer reaction and epoxidation. Furthermore, drastic counteranion effects in phase-transfer catalysis were observed for the first time, making it possible to three-dimensionally fine-tune the catalyst (ketal part, aromatic part, and counteranion). Copyright