187527-00-0

Basic information

• Product Name: [(S)-1-(4-tert-Butoxy-benzyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester
• Synonyms: [(S)-1-(4-tert-Butoxy-benzyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester
• CAS NO: 187527-00-0
• Molecular Weight: 574.676
• Mol File: 187527-00-0.mol

Chemical Properties

• CAS DataBase Reference: [(S)-1-(4-tert-Butoxy-benzyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(S)-1-(4-tert-Butoxy-benzyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester(187527-00-0)
• EPA Substance Registry System: [(S)-1-(4-tert-Butoxy-benzyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester(187527-00-0)

Safety Data

• Hazardous Substances Data: 187527-00-0(Hazardous Substances Data)

Upstream product

• 136918-14-4 phthalimide 
• 187526-99-4 (9H-fluoren-9-yl)methyl (S)-(1-(4-(tert-butoxy)phenyl)-3-hydroxypropan-2-yl)carbamate 
• 71989-38-3 Fmoc-Tyr(tBu)-OH 

Downstream Products

• 187527-06-6 ((S)-1-{3-[(S)-1-(3-{2-[3-(2-{3-[(S)-1-Aminomethyl-2-(4-hydroxy-phenyl)-ethyl]-ureido}-ethyl)-ureido]-ethyl}-ureidomethyl)-2-phenyl-ethyl]-ureidomethyl}-3-methyl-butyl)-urea 
• 869736-04-9 C₂₇H₃₇N₅O₄S₂ 
• 869735-99-9 2-[2-azido-3-(4-tert-butoxy-phenyl)-propyl]-isoindole-1,3-dione 
• 187527-01-1 2-[(S)-2-Amino-3-(4-tert-butoxy-phenyl)-propyl]-isoindole-1,3-dione 

Relevant articles and documents

Solid phase syntheses of oligoureas

Isocyanates 7 were formed from monoprotected diamines 3 or 6, which in turn can be easily prepared from commercially available N-BOC- or N-FMOC-protected amino acid derivatives. Isocyanates 7, formed in situ, could be coupled directly to a solid support f

Solid-phase and solution-phase syntheses of oligomeric guanidines bearing peptide side chains

Synthetic strategies for preparing N,N′-bridged oligomeric guanidines bearing peptide side chains both on solid support and in solution are presented. Monomers are prepared from common α-amino acids and therefore contain conventionally protected peptide s