Boc-Leu-OH.H2O
Suppliers
Names
[ CAS No. ]:
13139-15-6
[ Name ]:
Boc-Leu-OH.H2O
[Synonym ]:
N-Boc-L-leucine hydrate
(E)-N-{Hydroxy[(2-methyl-2-propanyl)oxy]methylene}-L-leucine
(S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid
MFCD00066067
L-LEUCINE-N-T-BOC:H2O
L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-
BOC-LEU
boc-leu-oh.h20
EINECS 236-073-2
N-tert-butoxycarbonyl-L-leucine
BOC-L-LEUCINE-OH
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-leucine
N-tert-butyloxycarbonyl-L-leucine
BOC-L-Leucine
N(alpha)-t-butoxycarbonyl-L-leucine
Boc-Leu-OH,H2O
Boc-Leu-OH.H2O
N-Boc-L-leucine Monohydrate
L-Leucine, N-[(1,1-dimethylethoxy)hydroxymethylene]-, (E)-
BOC-L-LEU-OH
BOC-LEU-OH
N-(tert-Butoxycarbonyl)-L-leucine Monohydrate
Boc-Leu-OH Monohydrate
N-Boc-L-leucine
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
339.7±44.0 °C at 760 mmHg
[ Melting Point ]:
85-87 °C
[ Molecular Formula ]:
C11H21NO4
[ Molecular Weight ]:
231.289
[ Flash Point ]:
159.2±28.4 °C
[ Exact Mass ]:
231.147064
[ PSA ]:
75.63000
[ LogP ]:
2.99
[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C
[ Index of Refraction ]:
1.472
[ Storage condition ]:
−20°C
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi,Xn
[ Risk Phrases ]:
R20/21/22
[ Safety Phrases ]:
26-36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2924199090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924199090
[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Nat. Chem. Biol. 5 , 45-52, (2009)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...
Anal. Chim. Acta 865 , 53-9, (2015)
Polydimethylsiloxane (PDMS) is widely used for microfabrication and bioanalysis; however, its surface functionalization is limited due to the lack of active functional groups and incompatibility with ...
J. Org. Chem. 74(19) , 7566-9, (2009)
The enantioselective total synthesis of PM-94128, a potent cytotoxin of microbial origin, was accomplished by a concise nine-step sequence of reactions in 14% overall yield from N-Boc-l-leucine. The s...