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[ CAS No. 14123-76-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 14123-76-3
Chemical Structure| 14123-76-3
Structure of 14123-76-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 14123-76-3 ]

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Product Details of [ 14123-76-3 ]

CAS No. :14123-76-3 MDL No. :MFCD11110658
Formula : C10H8ClN Boiling Point : No data available
Linear Structure Formula :- InChI Key :VLPNHJHAQSABQP-UHFFFAOYSA-N
M.W : 177.63 Pubchem ID :20616787
Synonyms :

Calculated chemistry of [ 14123-76-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.1
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 51.72
TPSA : 12.89 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.03 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.24
Log Po/w (XLOGP3) : 3.31
Log Po/w (WLOGP) : 3.2
Log Po/w (MLOGP) : 2.44
Log Po/w (SILICOS-IT) : 3.56
Consensus Log Po/w : 2.95

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.64
Solubility : 0.0404 mg/ml ; 0.000227 mol/l
Class : Soluble
Log S (Ali) : -3.26
Solubility : 0.0984 mg/ml ; 0.000554 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.7
Solubility : 0.00354 mg/ml ; 0.0000199 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.24

Safety of [ 14123-76-3 ]

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

Application In Synthesis of [ 14123-76-3 ]

* 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.

  • Upstream synthesis route of [ 14123-76-3 ]

[ 14123-76-3 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 919994-55-1 ]
  • [ 14123-76-3 ]
YieldReaction ConditionsOperation in experiment
76% at 130 - 140℃; for 3.16667 h; During 10 min. (4-chloro-benzyl)-[2,2-dimethoxy-1-methyl-eth-(Z)-ylidene]-amine (120 g, 0.496 mol) was added dropwise to polyphosphoric acid (1000 g) at 130 0C. The resulting reaction mixture was heated for 3 h at 140 0C. After cooling below 100 0C the reaction mixture was poured onto ice (1 kg) and neutralized (pH = 7) with a 33 percent aqueous NaOH solution. Care was taken that the temperature did not rise above 35 0C by adding additional ice. The reaction mixture was extracted with dichloromethane (3 x 1 L) and the combined organic layers were dried over Na2SO4, filtered and concentrated at reduced pressure to afford a black oil. The crude product was purified bulb-to-bulb distillation (105 -110 0C, 2 mbar) to afford the title compound as colorless oil which crystallized upon standing (66.7 g, 0.375 mol, 76percent). MS (ES+): 178 (M(C10H835CIN)+H)+.
Reference: [1] Patent: WO2007/6533, 2007, A2, . Location in patent: Page/Page column 32
  • 2
  • [ 108-22-5 ]
  • [ 80055-48-7 ]
  • [ 14123-76-3 ]
Reference: [1] Chemical Communications, 2015, vol. 51, # 68, p. 13327 - 13329
  • 3
  • [ 104-86-9 ]
  • [ 14123-76-3 ]
Reference: [1] Patent: WO2016/83816, 2016, A1,
  • 4
  • [ 6342-56-9 ]
  • [ 104-86-9 ]
  • [ 14123-76-3 ]
Reference: [1] Journal of Medicinal Chemistry, 2014, vol. 57, # 17, p. 7412 - 7424
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