L-tert-Leucine
Names
[ CAS No. ]:
20859-02-3
[ Name ]:
L-tert-Leucine
[Synonym ]:
MFCD00002617
L-Tert-Leucine
3-Methyl-L-valine
L-Valine, 3-methyl-
L-tert-leucin
L-2-tert-Butylglycine
Valine, 3-methyl-
(S)-2-Amino-3,3-dimethylbutyric acid
LEUCINE,L
(S)-2-Amino-3,3-dimethylbutanoic acid
3-Methyl valine
EINECS 200-522-0
3-Methylvaline
(S)-2-Amino-4-methylpentanoic acid
L-α-tert-Butylglycine
T-BUTYL GLYCINE
L-tert
H-L-LEU-OH
QVYZX1&1&1 &&L or S Form
L-2-amino-3,3-dimethylbutanoic acid
(2S)-2-amino-3,3-dimethylbutanoic acid
L-Tert-Leu-OH
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
[References]
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
217.7±23.0 °C at 760 mmHg
[ Melting Point ]:
300 °C
[ Molecular Formula ]:
C6H13NO2
[ Molecular Weight ]:
131.173
[ Flash Point ]:
85.5±22.6 °C
[ Exact Mass ]:
131.094635
[ PSA ]:
63.32000
[ LogP ]:
0.55
[ Vapour Pressure ]:
0.1±0.9 mmHg at 25°C
[ Index of Refraction ]:
1.464
[ Water Solubility ]:
125.5 g/L (20 ºC)
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi: Irritant;
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
OH2850000
[ HS Code ]:
2922499990
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2922499990
[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%
Articles
Org. Lett. 6 , 23-25, (2004)
[reaction: see text] A highly diastereoselective acetate aldol reaction that uses a tert-leucine-derived thiazolidinethione auxiliary and dichlorophenylborane has been developed. The reaction proceeds...
Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids.Nature 461(7266) , 968-70, (2009)
Alpha-amino acids are the building blocks of proteins and are widely used as components of medicinally active molecules and chiral catalysts. Efficient chemo-enzymatic methods for the synthesis of ena...
An efficient and selective enzymatic oxidation system for the synthesis of enantiomerically pure D-tert-leucine.Org. Lett. 5(20) , 3649-50, (2003)
[reaction: see text] d-tert-Leucine was prepared with an enantiomeric excess of >99% by an enzyme-catalyzed oxidative resolution of the racemic mixture of dl-tert-leucine with use of leucine dehydroge...