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[ CAS No. 17664-93-6 ] {[proInfo.proName]}

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Chemical Structure| 17664-93-6
Chemical Structure| 17664-93-6
Structure of 17664-93-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 17664-93-6 ]

CAS No. :17664-93-6 MDL No. :MFCD00066116
Formula : C20H27NO5S Boiling Point : No data available
Linear Structure Formula :C6H13NO2C7H6·C7H7SO3H InChI Key :QTQGHKVYLQBJLO-UTONKHPSSA-N
M.W : 393.50 Pubchem ID :44629929
Synonyms :
Chemical Name :H-D-Leu-OBzl.TosOH

Calculated chemistry of [ 17664-93-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 27
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.35
Num. rotatable bonds : 7
Num. H-bond acceptors : 6.0
Num. H-bond donors : 2.0
Molar Refractivity : 105.51
TPSA : 115.07 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.86 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.23
Log Po/w (XLOGP3) : 1.18
Log Po/w (WLOGP) : 4.27
Log Po/w (MLOGP) : 2.96
Log Po/w (SILICOS-IT) : 2.34
Consensus Log Po/w : 2.79

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.89
Solubility : 0.507 mg/ml ; 0.00129 mol/l
Class : Soluble
Log S (Ali) : -3.19
Solubility : 0.253 mg/ml ; 0.000642 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.42
Solubility : 0.151 mg/ml ; 0.000384 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.45

Safety of [ 17664-93-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 17664-93-6 ]

* 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 [ 17664-93-6 ]

[ 17664-93-6 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 2130-96-3 ]
  • [ 17664-93-6 ]
  • [ 66959-93-1 ]
  • 2
  • [ 59969-65-2 ]
  • [ 17664-93-6 ]
  • [ 62058-27-9 ]
  • 3
  • [ 62023-58-9 ]
  • [ 17664-93-6 ]
  • [ 62058-31-5 ]
  • 4
  • [ 17664-93-6 ]
  • [ 62023-60-3 ]
  • (R)-2-((2R,3S)-3-Benzyloxycarbonylamino-2-hydroxy-4-phenyl-butyrylamino)-4-methyl-pentanoic acid benzyl ester [ No CAS ]
  • 5
  • [ 17664-93-6 ]
  • [ 62023-59-0 ]
  • [ 62058-29-1 ]
  • 6
  • [ 5292-43-3 ]
  • [ 17664-93-6 ]
  • (R)-2-(tert-Butoxycarbonylmethyl-amino)-4-methyl-pentanoic acid benzyl ester; compound with toluene-4-sulfonic acid [ No CAS ]
  • 7
  • [ 37553-65-4 ]
  • [ 17664-93-6 ]
  • (R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-3-phenyl-propionylamino]-4-methyl-pentanoic acid benzyl ester [ No CAS ]
  • 8
  • [ 13748-90-8 ]
  • [ 17664-93-6 ]
  • [ 184034-25-1 ]
  • 9
  • [ 3303-84-2 ]
  • [ 17664-93-6 ]
  • [ 223270-78-8 ]
  • 10
  • [ 17664-93-6 ]
  • [ 124072-61-3 ]
  • [ 223270-79-9 ]
YieldReaction ConditionsOperation in experiment
99% D-Leucine O-benzyl ester Tosylate salt To benzyl alcohol (8.2 g) dissolved in benzene (30 mL) was added D-leucine (5.0 g) and p-toluenesulfonic acid monohydrate (8.0 g). The reaction was warmed to reflux with removal of water overnight. Once TLC indicated consumption of starting material, the reaction was cooled, and the resulting solid was filtered and washed with EtOAc to give the title compound as a white powder (14.26 g, 99%).
73% A. Benzyl D-Leucinate p-Toluenesulfonate This compound was prepared in a manner corresponding precisely to that described in Part A of Example 1 for preparation of the D-alinate compound. Yield, 73%, m.p. 155-156 C. Analysis, calculated for C20 H27 NO5 S (393.50): C, 61.05; H, 6.92; N, 3.56. Found: C, 61.17; H, 6.68; N, 3.81.
  • 12
  • [ 98-01-1 ]
  • [ 17664-93-6 ]
  • (R)-2-[1-Furan-2-yl-meth-(E)-ylidene]-amino}-4-methyl-pentanoic acid benzyl ester [ No CAS ]
  • 13
  • [ 17664-93-6 ]
  • [ 100-52-7 ]
  • (R)-4-Methyl-2-[1-phenyl-meth-(E)-ylidene]-amino}-pentanoic acid benzyl ester [ No CAS ]
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