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[ CAS No. 7517-19-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 7517-19-3
Chemical Structure| 7517-19-3
Structure of 7517-19-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 7517-19-3 ]

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Product Details of [ 7517-19-3 ]

CAS No. :7517-19-3 MDL No. :MFCD00012494
Formula : C7H16ClNO2 Boiling Point : -
Linear Structure Formula :[H3NCH(CH2CH(CH3)2)CO2CH3]Cl InChI Key :DODCBMODXGJOKD-RGMNGODLSA-N
M.W : 181.66 Pubchem ID :2723695
Synonyms :
Chemical Name :H-Leu-OMe.HCl

Calculated chemistry of [ 7517-19-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.72
TPSA : 52.32 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.18 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.73
Log Po/w (WLOGP) : 1.33
Log Po/w (MLOGP) : 1.08
Log Po/w (SILICOS-IT) : 0.4
Consensus Log Po/w : 0.91

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.79
Solubility : 2.93 mg/ml ; 0.0161 mol/l
Class : Very soluble
Log S (Ali) : -2.45
Solubility : 0.652 mg/ml ; 0.00359 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.85
Solubility : 25.6 mg/ml ; 0.141 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.83

Safety of [ 7517-19-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 7517-19-3 ]

* 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 [ 7517-19-3 ]

[ 7517-19-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 13211-32-0 ]
  • [ 7517-19-3 ]
  • [ 16071-39-9 ]
  • 2
  • [ 954147-36-5 ]
  • [ 7517-19-3 ]
  • Fmoc-Glu(tetrazole)-Leu-OMe [ No CAS ]
  • 3
  • [ 7517-19-3 ]
  • [ 52558-24-4 ]
  • C15H28N2O6 [ No CAS ]
  • 4
  • [ 7517-19-3 ]
  • [ 53308-95-5 ]
  • [ 78664-45-6 ]
YieldReaction ConditionsOperation in experiment
75% With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20℃; General procedure: To a cooled solution of Boc-L-leucine (1.0 equiv.), the amine/alpha-aminoester HCl (1.2-1.5 equiv.), and PyBop 1.2 equiv. (or EDCI*HCl1.2 equiv. and HOBt 1.2 equiv.) in anhydrous DMF was added diisopropylethylamine (3.3-4.0 equiv.) gradually. The reaction mixture was stirred at room temperature for 5 h to overnight, diluted with ethyl acetate (50 mL for every 5 mL DMF), then extracted with 1 M HCl (3), saturated sodium bicarbonate (3), and brine (2). The organic layer was then dried with anhydrous sodium sulfate and the solvent was evaporated under vacuum to give the products which were purified by flash chromatography whenever needed.
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