Boc-D-Leu-OH.H2O

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Names

[ CAS No. ]:
16937-99-8

[ Name ]:
Boc-D-Leu-OH.H2O

[Synonym ]:
MFCD00038294
BOC-D-Leucinemonohydrate
Boc-D-Leu-OH&BOC-D-LEU
N-BOC-D-Leucine.H2O
Boc-D-Leu-OH Hydrate
N-(tert-Butoxycarbonyl)-D-leucine
D-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-, hydrate (1:1)
BOC-D-LEUCINE-OH
N-T-BOC-D-LEUCINE
Boc-D-Leu-OH
N-(tert-Butoxycarbonyl)-D-leucine hydrate (1:1)
N-(tert-Butoxycarbonyl)-D-leucine Hydrate
BOC-D-LEU-OH2O
N-tert-butoxycarbonyl-D-leucine
n-boc-d-leucine
N-Boc-D-leucine Hydrate
D-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-
tert-butoxycarbonyl-D-leucine
N-(t-butyloxycarbonyl)-D-leucine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-leucine hydrate (1:1)
Boc-D-Leu-OH.H2O
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-leucine
BOC-D-LEUCINE
Boc-(R)-leucine

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
356.0±25.0 °C at 760 mmHg

[ Melting Point ]:
85-87ºC(lit.)

[ Molecular Formula ]:
C11H21NO4

[ Molecular Weight ]:
231.289

[ Flash Point ]:
169.1±23.2 °C

[ Exact Mass ]:
231.147064

[ PSA ]:
84.86000

[ LogP ]:
2.51

[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C

[ Index of Refraction ]:
1.461

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • H-D-Leu-OH
  • Di-tert-butyl dicarbonate
  • 2-[[(tert-butoxycarbonyl)oxy]imino]-2-phenylacetonitrile
  • D-Allylglycine
  • (R)-2-amino-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,4-dimethylpentanamide
  • N-Boc-D-leucinol

DownStream

  • H-D-Leu-OH
  • Boc-N-methyl-D-leucine
  • N-Boc-D-leucinol
  • (s)-3-boc-amino-1-diazo-5-methyl-2-hexanone
  • (R)-Benzyl 2-amino-4-methylpentanoate hydrochloride

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

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

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...


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Related Compounds

  • Boc-D-Leu-OH.H2O
  • Boc-D-Leu-Phe-OH
  • Boc-D-Leu-OSu
  • Boc-D-Leu-Trp-Arg(Cbz)2-OBn
  • Boc-D-Leu-OPfp
  • Boc-D-Leu-L-His-OCH3
  • (2-Chloro-5-ethoxypyridin-4-yl)boronic acid
  • Ethyl 7-Chloroimidazo[1,2-b]pyridazine-2-carboxylate
  • Ethyl 3-bromo-8-hydroxyimidazo[1,2-b]pyridazine-7-carboxylate
  • (2R)-2-amino-1-(4,5-dihydrofuran-3-yl)butan-1-one
  • 3-(4-Bromophenyl)-4,5-dihydro-1-methyl-1H-pyrazole
  • 1-Chloro-4-sulfanylbutan-2-one
  • 2-(1-Phenylcyclopentyl)morpholine
  • 2-(3,4-Difluorophenyl)-1-(4-hydroxyphenyl)ethanone
  • 1,1-Difluoro-2,4-dimethyl-5-phenylpent-4-en-2-amine
  • Lactic acid, tetraester with silicic acid (H4SiO4)
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