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[ CAS No. 17295-11-3 ] {[proInfo.proName]}

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Chemical Structure| 17295-11-3
Chemical Structure| 17295-11-3
Structure of 17295-11-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 17295-11-3 ]

CAS No. :17295-11-3 MDL No. :MFCD00100526
Formula : C12H10O3 Boiling Point : -
Linear Structure Formula :- InChI Key :UKZOPQRTQJERQC-UHFFFAOYSA-N
M.W : 202.21 Pubchem ID :390995
Synonyms :

Calculated chemistry of [ 17295-11-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.08
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 57.25
TPSA : 46.53 ?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) : -6.04 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.02
Log Po/w (XLOGP3) : 2.11
Log Po/w (WLOGP) : 2.33
Log Po/w (MLOGP) : 2.31
Log Po/w (SILICOS-IT) : 2.34
Consensus Log Po/w : 2.22

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.78
Solubility : 0.332 mg/ml ; 0.00164 mol/l
Class : Soluble
Log S (Ali) : -2.72
Solubility : 0.387 mg/ml ; 0.00191 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.58
Solubility : 0.0532 mg/ml ; 0.000263 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.1

Safety of [ 17295-11-3 ]

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

Application In Synthesis of [ 17295-11-3 ]

* 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 [ 17295-11-3 ]

[ 17295-11-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17295-11-3 ]
  • [ 3290-06-0 ]
  • [ 1548149-23-0 ]
YieldReaction ConditionsOperation in experiment
1.74 g With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 1h; Potassium carbonate (3.28 g, 23.7 mmol) was added to a solution of 6-hydroxy-naphthalene-2-carboxylic acid methyl ester (2.00 g, 9.89 mmol) in N,N-dimethyl-formamide (25 mL), followed by l,3-dichloro-5-chloromethyl-benzene (2.51 g, 12.8 mmol). Stirred at 50 C for lh. Cooled to rt and diluted with ethyl acetate and washed with water (5x). The organics were dried and concentrated. The white solid was then washed with ethyl acetate and dried to give the title compound as a white powder (1.74g). LCMS: RT 2.27 min; MH+ 361. 1H NMR (300 MHz, CHLOROFORM-d) delta 8.51 - 8.59 (m, 1H), 8.05 (dd, J = 1.51, 8.69 Hz, 1H), 7.90 (d, J = 8.69 Hz, 1H), 7.76 (d, J = 8.31 Hz, 1H), 7.39 (d, J = 1.89 Hz, 2H), 7.33 - 7.37 (m, 1H), 7.30 (d, J = 2.64 Hz, 1H), 7.20 (d, J = 2.27 Hz, 1H), 5.16 (s, 2H), 3.93 - 4.03 (m, 3H).
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