107496-46-8

Basic information

• Product Name: N^α-(tert-butyloxycarbonyl)-DL-hexafluorovaline
• CAS NO: 107496-46-8
• Molecular Weight: 325.208
• Mol File: 107496-46-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N^α-(tert-butyloxycarbonyl)-DL-hexafluorovaline(CAS DataBase Reference)
• NIST Chemistry Reference: N^α-(tert-butyloxycarbonyl)-DL-hexafluorovaline(107496-46-8)
• EPA Substance Registry System: N^α-(tert-butyloxycarbonyl)-DL-hexafluorovaline(107496-46-8)

Safety Data

• Hazardous Substances Data: 107496-46-8(Hazardous Substances Data)

Upstream product

• 34619-03-9 tert-butyldicarbonate 
• 16063-80-2 (RS)-hexafluorovaline 
• 107496-44-6 benzyl 4,4,4-trifluoro-3-(trifluoromethyl)but-2-enoate 
• 107496-45-7 DL-hexafluorovaline benzyl ester 
• 78185-92-9 DL-Hfv-OEt 
• 1513-60-6 ethyl 4,4,4-trifluoro-3-(trifluoromethyl)crotonate 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1098184-03-2 C₁₀H₁₃F₆NO₄ 

Relevant articles and documents

Synthesis of [Hexafluorovalyl1,1′]gramicidin S

[Hexafluorovalyl1,1′]gramicidin S (8), in which two valine residues in the natural gramicidin S were replaced by L-hexafluorovaline (Hfv) residues, was synthesized by the solid-phase-synthesis and cyclization-cleavage method on benzophenone oxime resin. Though the racemic hexafluorovaline derivative was employed for the peptide synthesis, the desired product was isolated in moderate yield, probably reflecting the stable cyclic structure of 8. CD and 1HNMR spectra indicated that the conformation of 8 is similar to that of gramicidin S. The two β-turn structure and antiparallel β-sheet structure with four intramolecular hydrogen bondings were maintained in spite of introducing the hexafluorovaline residues. The dye-release experiment from lecithin vesicle and antimacrobial activity assay also indicated that 8 showed membrane-disturbing activity like gramicidin S, although the activity of 8 was somewhat weaker than gramicidin S.

Substituted hydantoins

The present invention relates to compounds of the formula methods for the preparation thereof, and methods for their use. The compounds are useful in treating diseases characterized by the hyperactivity of MEK. Accordingly the compounds are useful in the treatment of diseases, such as cancer, cognitive and CNS disorders, and inflammatory/autoimmune diseases.