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[ CAS No. 103987-81-1 ] {[proInfo.proName]}

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Chemical Structure| 103987-81-1
Chemical Structure| 103987-81-1
Structure of 103987-81-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 103987-81-1 ]

CAS No. :103987-81-1 MDL No. :MFCD08703597
Formula : C11H7N Boiling Point : -
Linear Structure Formula :- InChI Key :PBKFDEMENCIDDQ-UHFFFAOYSA-N
M.W : 153.18 Pubchem ID :53338769
Synonyms :

Calculated chemistry of [ 103987-81-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.68
TPSA : 12.89 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.11
Log Po/w (XLOGP3) : 2.48
Log Po/w (WLOGP) : 2.3
Log Po/w (MLOGP) : 2.36
Log Po/w (SILICOS-IT) : 3.12
Consensus Log Po/w : 2.47

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.97
Solubility : 0.165 mg/ml ; 0.00107 mol/l
Class : Soluble
Log S (Ali) : -2.4
Solubility : 0.616 mg/ml ; 0.00402 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.77
Solubility : 0.0263 mg/ml ; 0.000171 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.59

Safety of [ 103987-81-1 ]

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

Application In Synthesis of [ 103987-81-1 ]

* 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 [ 103987-81-1 ]
  • Downstream synthetic route of [ 103987-81-1 ]

[ 103987-81-1 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 869208-50-4 ]
  • [ 103987-81-1 ]
YieldReaction ConditionsOperation in experiment
80% With sodium hydroxide In toluene at 120℃; for 0.5 h; 8.5 g (40 mmol) of Dimethylhydroxymethyl-8-quinolylacetylene and 1. g (45 mmol) of sodium hydroxide (manufactured by KISHIDA CHEMICAL CO., Ltd., 0.7 mm granular, 98percent) were placed in a 300 mL two-neck flask equipped with a reflux condenser and the air inside the flask was replaced with argon gas. 200 mL of toluene was added thereto and the mixture was refluxed at 120°C for 0.5 hours. Diethyl ether was added to the reaction mixture, the mixture was washed with a saturated aqueous ammonium chloride solution and dried over magnesium sulfate, and then the solvent was distilled off under reduced pressure by an evaporator. Hexane (250 ml) was added to the residue and the mixture was heated to 70°C. After filtering out the insolubles, the desired compound precipitated by cooling it to -78°C was filtered and washed with cold hexane (-78°C; 100 ml) and then dried under reduced pressure to give 4.9 g of the desired compound as a yellowish white solid (yield: 80percent). 1H-NMR (300 MHz, CDCl3) δ: 3.60 (s, 1H), 7.32-7.53 (m, 2H), 7.83 (dd, 1H), 7.93 (dd, 1H), 8.17 (dd, 1H), 9.06-9.08 (m, 1H) EI-MS (M/Z) : 153(M+-1), CI-MS(M/Z): 154 (MH+)
Reference: [1] Patent: EP1847545, 2007, A1, . Location in patent: Page/Page column 35-36
  • 2
  • [ 895164-50-8 ]
  • [ 103987-81-1 ]
Reference: [1] Dalton Transactions, 2006, # 19, p. 2288 - 2290
  • 3
  • [ 148-24-3 ]
  • [ 103987-81-1 ]
Reference: [1] Dalton Transactions, 2006, # 19, p. 2288 - 2290
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