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[ CAS No. 131980-30-8 ] {[proInfo.proName]}

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Chemical Structure| 131980-30-8
Chemical Structure| 131980-30-8
Structure of 131980-30-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 131980-30-8 ]

CAS No. :131980-30-8 MDL No. :MFCD00797560
Formula : C15H18N2O4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :FDQDHMZKOPOWFE-LBPRGKRZSA-N
M.W : 290.31 Pubchem ID :2734498
Synonyms :

Calculated chemistry of [ 131980-30-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 21
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.4
Num. rotatable bonds : 7
Num. H-bond acceptors : 5.0
Num. H-bond donors : 2.0
Molar Refractivity : 76.06
TPSA : 99.42 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.05
Log Po/w (XLOGP3) : 2.23
Log Po/w (WLOGP) : 2.08
Log Po/w (MLOGP) : 1.33
Log Po/w (SILICOS-IT) : 1.71
Consensus Log Po/w : 1.88

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.79
Solubility : 0.466 mg/ml ; 0.00161 mol/l
Class : Soluble
Log S (Ali) : -3.95
Solubility : 0.0323 mg/ml ; 0.000111 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.25
Solubility : 0.161 mg/ml ; 0.000556 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.87

Safety of [ 131980-30-8 ]

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 [ 131980-30-8 ]

* 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.

  • Upstream synthesis route of [ 131980-30-8 ]

[ 131980-30-8 ] Synthesis Path-Upstream   1~6

  • 1
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  • [ 131980-30-8 ]
Reference: [1] Patent: WO2006/42678, 2006, A1, . Location in patent: Page/Page column 12
[2] Patent: WO2004/101507, 2004, A2, . Location in patent: Page/Page column 51
  • 2
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Reference: [1] Patent: US2007/55065, 2007, A1,
  • 3
  • [ 24424-99-5 ]
  • [ 131980-30-8 ]
Reference: [1] Patent: US2003/21773, 2003, A1,
  • 4
  • [ 74651-77-7 ]
  • [ 131980-30-8 ]
YieldReaction ConditionsOperation in experiment
81% With N-ethyl-N,N-diisopropylamine In 1,4-dioxane; water Boc-3-cyano-(L)-phenylalanine
6 g (26.5 mmol) of 3-cyano-(L)-phenylalanine hydrochloride and 9.1 ml (53.2 mmol) of N-ethyldiisopropylamine was suspended in 17 ml of water.
To this suspension was added a solution of 7.2 g (29.2 mmol) of 2-(Boc-oxyimino)-2-phenylacetonitrile in 20 ml of dioxane and stirring continued for 16 hours at room temperature.
After subsequent addition of 50 ml of water, the solution was extracted with 50 ml of ethyl acetate, the organic phase separated and the pH of the aqueous phase adjusted to 3 with dilute hydrochloric acid.
After 3 extractions with 100 ml each of ethyl acetate, the collected organic solutions were washed with saturated sodium chloride solution, dried over magnesium sulfate and the solvent was evaporated under reduced pressure.
Yield: 6.2 g (81percent)
Reference: [1] Patent: US5607937, 1997, A,
  • 5
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Reference: [1] Patent: US5750520, 1998, A,
  • 6
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  • [ 131980-30-8 ]
Reference: [1] Journal of Medicinal Chemistry, 2012, vol. 55, # 3, p. 1171 - 1180
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