1357067-24-3

Basic information

• Product Name: C₁₇H₂₅NO₄
• Synonyms: C₁₇H₂₅NO₄
• CAS NO: 1357067-24-3
• Molecular Weight: 307.39
• Mol File: 1357067-24-3.mol

Chemical Properties

• CAS DataBase Reference: C₁₇H₂₅NO₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₂₅NO₄(1357067-24-3)
• EPA Substance Registry System: C₁₇H₂₅NO₄(1357067-24-3)

Safety Data

• Hazardous Substances Data: 1357067-24-3(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 10433-52-0 O-benzyl-D-serine 
• 1826-67-1 vinyl magnesium bromide 
• 79069-15-1 N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol 
• 108149-63-9 4-hydroxymethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 100-39-0 benzyl bromide 
• 1339950-10-5 (R)-tert-butyl 4-((benzyloxy)methyl)-2,2-dimethyloxazolidine-3-carboxylate 

Relevant articles and documents

NOVEL COMPOUNDS FOR MEDICAL USE AS PEPTIDASE EFFECTORS

The invention relates to compounds of general formula (I) as set forth in the claims as well as to the use of the compounds of the general formula (1) in the medical field, specifically for use in the suppression of DNA synthesis and inflammatory cytokine production as well as in the stimulation of anti-inflammatory cytokine production in vitro and in vivo. This abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.

A stereoselective route to cis-(2S,3R)-3-hydroxypipecolic acid and two enantiomeric cis-2-hydroxymethyl-3-hydroxypiperidine derivatives

Stereoselective routes to cis-(2S,3R)-3-hydroxypipecolic acid and two enantiomeric cis-2-hydroxymethyl-3-hydroxypiperidine derivatives from a common precursor have been developed, which featured stereocontrolled vinylation of a -chiral aldehyde and ring-closing metathesis as key steps. Georg Thieme Verlag Stuttgart. New York.