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Chemical Structure| 2743-40-0 Chemical Structure| 2743-40-0
Chemical Structure| 2743-40-0

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L-Leucine Ethyl Ester HCl is a leucine derivative, commonly used in peptide synthesis and drug chemistry research.

Synonyms: H-Leu-OEt.HCl

4.5 *For Research Use Only !

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Product Details of L-Leucine Ethyl Ester HCl

CAS No. :2743-40-0
Formula : C8H18ClNO2
M.W : 195.69
SMILES Code : Cl[H].[H][C@](N)(CC(C)C)C(=O)OCC
Synonyms :
H-Leu-OEt.HCl
MDL No. :MFCD00034879
InChI Key :NOUDPBCEONUCOV-FJXQXJEOSA-N
Pubchem ID :11658447

Safety of L-Leucine Ethyl Ester HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of L-Leucine Ethyl Ester HCl

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 2743-40-0 ]

[ 2743-40-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2743-40-0 ]
  • [ 156047-39-1 ]
YieldReaction ConditionsOperation in experiment
With tetrakis(tetrabutylammonium)decatungstate(VI); N-fluorobis(benzenesulfon)imide; In water; acetonitrile; for 66h;Inert atmosphere; Sealed tube; UV-irradiation; [0078] On a larger scale, a solution of (L)-leucine ethyl ester hydrochloride salt (100 mg, 0.51 mmol), TBADT (37 mg, 2%) and NFSI (193 mg, 0.61 mmol) in CH3CN/H20 (2: 1, 6.0 mL) was purged with nitrogen (10 minutes) then sealed. The resulting solution was then placed between two 15 watt UVB (365 nm) lamps and irradiated for 18 hours. At this time, another aliquot of solid NFSI (75 mg) was added to the solution and it was purged with nitrogen for another 10 minutes. The resulting solution was irradiated between two 15 watt UVB (365 nm) lamps for another 24 hours. At this time more solid NFSI (50 mg) was added to the solution and it was purged with nitrogen for another 10 min, and irradiated for a further 24 hours, and then worked up as follows: The blue solution was diluted with CHC13 and water/potassium carbonate was added to pH >10. The solvent was removed via rotary evaporator and the resulting white solid was suspended in CHCI3 and dried over MgSC>4. The solution was cooled in a freezer and then filtered over celite, washing with cold CHCI3. Concentration of the filtrate yielded an orange oil (68 mg) that was -75% pure based on H NMR analysis. The approximate isolated yield of (
 

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