433922-97-5

Basic information

• Product Name: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-N-trityl-succinamic acid 1-{[tert-butoxycarbonyl-(2-tert-butoxycarbonyl-1-isopropylcarbamoyl-ethyl)-amino]-methyl}-4-methyl-2-(2,4,6-trimethyl-benzenesulfonylamino)-pentyl ester
• CAS NO: 433922-97-5
• Molecular Weight: 1220.54
• Mol File: 433922-97-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-N-trityl-succinamic acid 1-{[tert-butoxycarbonyl-(2-tert-butoxycarbonyl-1-isopropylcarbamoyl-ethyl)-amino]-methyl}-4-methyl-2-(2,4,6-trimethyl-benzenesulfonylamino)-pentyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-N-trityl-succinamic acid 1-{[tert-butoxycarbonyl-(2-tert-butoxycarbonyl-1-isopropylcarbamoyl-ethyl)-amino]-methyl}-4-methyl-2-(2,4,6-trimethyl-benzenesulfonylamino)-pentyl ester(433922-97-5)
• EPA Substance Registry System: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-N-trityl-succinamic acid 1-{[tert-butoxycarbonyl-(2-tert-butoxycarbonyl-1-isopropylcarbamoyl-ethyl)-amino]-methyl}-4-methyl-2-(2,4,6-trimethyl-benzenesulfonylamino)-pentyl ester(433922-97-5)

Safety Data

• Hazardous Substances Data: 433922-97-5(Hazardous Substances Data)

Upstream product

• 132388-59-1 L-Asn(Trt) 
• 433922-96-4 3-{tert-butoxycarbonyl-[2-hydroxy-5-methyl-3-(2,4,6-trimethyl-benzenesulfonylamino)-hexyl]-amino}-N-isopropyl-succinamic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 433922-92-0 2,4,6-Trimethyl-N-((R)-3-methyl-1-(R)-oxiranyl-butyl)-benzenesulfonamide 
• 433922-90-8 (2S,3R)-2-(tert-Butyl-dimethyl-silanyloxymethyl)-3-isobutyl-1-(2,4,6-trimethyl-benzenesulfonyl)-aziridine 
• 433922-95-3 3-[2-hydroxy-5-methyl-3-(2,4,6-trimethyl-benzenesulfonylamino)-hexylamino]-N-isopropyl-succinamic acid tert-butyl ester 

Relevant articles and documents

Efficient stereoselective synthesis of peptidomimetics containing hydroxyethylamine dipeptide isosteres utilizing the aza-Payne rearrangement and O, N-acyl transfer reactions

A novel methodology utilizing the aza-Payne rearrangement and O, N-intramolecular acyl transfer reactions for the synthesis of peptidomimetics containing hydroxyethylamine dipeptide isosteres (HDIs) is described. This methodology is useful for the stereos