ChemicalBook > Product Catalog > Biochemical Engineering > Amino Acids and Derivatives > Leucine derivatives > Z-TLE-OH DCHA
Z-TLE-OH DCHA
Z-TLE-OH DCHA Basic information
- Product Name:
- Z-TLE-OH DCHA
- Synonyms:
-
- 3-Methyl-N-[(phenylmethoxy)carbonyl]-L-valine compd. with N-cyclohexylcyclohexanamine
- Z-L-tert-butyl-Gly-OH·DCHA
- Z-L-Tle-OH·DCHA
- (-)-N-Benzyloxycarbonyl-L-tert-leucine dicyclohexyl ammonium salt for synthesis
- N-ALPHA-CARBOBENZOXY-L-ALPHA-T-BUTYLGLYCINE DICYCLOHEXYLAMINE SALT
- N-ALPHA-CARBOBENZOXY-L-TERT-LEUCINE DICYCLOHEXYLAMINE SALT
- (-)-N-BENZYLOXYCARBONYL-L-TERT-LEUCINE DICYCLOHEXYLAMMONIUM SALT
- Z-ALPHA-T-BUTYL-GLY-OH DCHA
- CAS:
- 62965-37-1
- MF:
- C14H19NO4.C12H23N
- MW:
- 446.63
- EINECS:
- 478-250-9
- Mol File:
- 62965-37-1.mol
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Z-TLE-OH DCHA Chemical Properties
- Melting point:
- 163-167 °C
- Density
- 1.1 at 20℃
- vapor pressure
- 0Pa at 25℃
- storage temp.
- 2-8°C
- form
- Solid
- PH
- 6.3 (H2O, 20℃)(saturated solution)
- optical activity
- [α]20/D 6.5±1°, c = 1% in methanol
- BRN
- 3831936
- LogP
- 1.6 at 25℃ and pH2.5
- Surface tension
- 63mN/m at 1g/L and 20℃
MSDS
- Language:English Provider:SigmaAldrich
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Z-TLE-OH DCHA Usage And Synthesis
Uses
3-methyl-N-[(phenylmethoxy)carbonyl]-L-Valine, with N-cyclohexylcyclohexanamine is used in the preparation of an intermediate towards the interleukin-1β converting enzyme inhibitor VX-765 using the palladium-catalyzed coupling of a bromodihydrofuranone with Cbz-L-prolinamide as the key step.
Z-TLE-OH DCHASupplier
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