(R)-TERT-LEUCINOL
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(R)-TERT-LEUCINOL ??
- ???
- 30-33 °C(lit.)
- ?? ?
- 70 °C0.4 mm Hg(lit.)
- ??
- 0.9 g/mL at 25 °C(lit.)
- ???
- 194 °F
- ?? ??
- Keep in dark place,Inert atmosphere,2-8°C
- ??? ??
- ??
- ?? ?? (pKa)
- 12.88±0.10(Predicted)
- ??
- ??~??
- ??? (Optical Rotation)
- [α]20/D 37°, c = 1.5 in ethanol
- InChI
- InChI=1S/C6H15NO/c1-6(2,3)5(7)4-8/h5,8H,4,7H2,1-3H3/t5-/m0/s1
- InChIKey
- JBULSURVMXPBNA-YFKPBYRVSA-N
- SMILES
- C(O)[C@H](N)C(C)(C)C
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- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ????(GHS): |
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(R)-TERT-LEUCINOL C??? ??, ??, ??
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(R)-Tert-leucinol (H-D-Tle-ol) is a chiral molecular compound with optical activity and its enantiomeric form is (S)-tert-leucinol. (R)-Tert-leucinol belongs to the class of α-amino alcohols, which have certain biological activities and are potent reversible inhibitors of protein synthesis. (R)-Tert-leucinol can be used as a chiral ligand for asymmetric catalytic reactions. Its derivatives are also used as optical splitting reagents, for peptidyl alcohol synthesis in peptide drugs, and as inhibitors of protein hydrolysis.(R)-TERT-LEUCINOL ?? ?? ? ???
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(R)-TERT-LEUCINOL ?? ??
???( 196)?? ??
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(R)-TERT-LEUCINOL ?? ??:
????? ??? 3,3-????-1-???
Fmoc-L-tert-leucine
L-tert-Leucine
FMOC-D-ALPHA-T-BUTYLGLYCINE
(-)-CHIRACAMPHOX
METHYLLYCACONITINE CITRATE
BOC-D-ALPHA-T-BUTYLGLYCINE
L-tert-Leucine methyl ester hydrochloride
D-tert-Butylglycine
DELCORINE
(S)-(-)-4-TERT-BUTYL-2-OXAZOLIDINONE
(R)-(+)-4-TERT-BUTYL-2-OXAZOLIDINONE
Valrubicin
(R)-TERT-LEUCINOL
Cbz-L-tert-Leucine
(S,S)-2,2'-METHYLENEBIS(4-TERT-BUTYL-2-OXAZOLINE)
(S,S)-(-)-2,2'-ISOPROPYLIDENEBIS(4-TERT-BUTYL-2-OXAZOLINE)