357608-40-3

Basic information

• Product Name: (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-[4-(2-(naphthalen-2-yl)-2-oxo-ethoxy)-phenyl]-piperidine-1-carboxylate
• Synonyms: (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-[4-(2-(naphthalen-2-yl)-2-oxo-ethoxy)-phenyl]-piperidine-1-carboxylate
• CAS NO: 357608-40-3
• Molecular Weight: 630.579
• Mol File: 357608-40-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-[4-(2-(naphthalen-2-yl)-2-oxo-ethoxy)-phenyl]-piperidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-[4-(2-(naphthalen-2-yl)-2-oxo-ethoxy)-phenyl]-piperidine-1-carboxylate(357608-40-3)
• EPA Substance Registry System: (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-[4-(2-(naphthalen-2-yl)-2-oxo-ethoxy)-phenyl]-piperidine-1-carboxylate(357608-40-3)

Safety Data

• Hazardous Substances Data: 357608-40-3(Hazardous Substances Data)

Upstream product

• 357608-38-9 (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-(4-triisopropylsilanyloxy-phenyl)-piperidine-1-carboxylate 
• 357608-36-7 tert-butyl 4-[4-(tert-butyl-dimethyl-silanoxy)-phenyl]-3,4-dihydroxy-piperidine-1-carboxylate 
• 357608-37-8 (3R,4R)-3-Hydroxy-4-(4-triisopropylsilanyloxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester 
• 357608-35-6 tert-butyl 4-[4-(tert-butyl-dimethyl-silanoxy)-phenyl]-3,6-dihydro-2H-pyridine-1-carboxylate 
• 257938-67-3 tert-butyl (3R,4R)-3-hydroxy-4-(4-hydroxyphenyl)-piperidine-1-carboxylate 
• 159191-56-7 (4-((tert-butyldimethylsilyl)oxy)phenyl)boronic acid 
• 138647-49-1 4-Trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 79099-07-3 N-tert-butyloxycarbonylpiperidin-4-one 
• 67963-68-2 t-butyldimethylsilyl-4-bromophenol 
• 613-54-7 2-Bromo-2'-acetonaphthone 
• 357608-39-0 (R,R)-tert-butyl 3-(4-bromo-benzyloxy)-4-(4-hydroxy-phenyl)-piperidine-1-carboxylate 

Relevant articles and documents

From peptides to non-peptide peptidomimetics: design and synthesis of new piperidine inhibitors of aspartic peptidases.

[reaction: see text] The 3-alkoxy-4-arylpiperidine inhibitors of aspartic peptidases are shown to be a new type of non-peptide peptidomimetic inhibitor. These piperidines can be designed from peptide-derived inhibitors by use of a structure-generating pro