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[ CAS No. 14062-18-1 ] {[proInfo.proName]}

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Chemical Structure| 14062-18-1
Chemical Structure| 14062-18-1
Structure of 14062-18-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 14062-18-1 ]

CAS No. :14062-18-1 MDL No. :MFCD00040760
Formula : C11H14O3 Boiling Point : No data available
Linear Structure Formula :CH3OC6H4CH2COOC2H5 InChI Key :DOCCDOCIYYDLGJ-UHFFFAOYSA-N
M.W : 194.23 Pubchem ID :84174
Synonyms :

Calculated chemistry of [ 14062-18-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 53.61
TPSA : 35.53 ?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) : -5.89 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.21
Log Po/w (XLOGP3) : 2.25
Log Po/w (WLOGP) : 1.8
Log Po/w (MLOGP) : 1.96
Log Po/w (SILICOS-IT) : 2.43
Consensus Log Po/w : 2.13

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.45
Solubility : 0.691 mg/ml ; 0.00356 mol/l
Class : Soluble
Log S (Ali) : -2.63
Solubility : 0.453 mg/ml ; 0.00233 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.41
Solubility : 0.0749 mg/ml ; 0.000385 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.62

Safety of [ 14062-18-1 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P233-P240-P241+P242+P243-P280-P303+P361+P353-P370+P378-P403+P235-P501 UN#:1993
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 14062-18-1 ]

* 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.

  • Downstream synthetic route of [ 14062-18-1 ]

[ 14062-18-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 3913-23-3 ]
  • [ 14062-18-1 ]
  • C19H21NO6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium hexamethyldisilazane; In tetrahydrofuran; at -70 - 20℃; for 16h; EXAMPLE 7; 5-(2-furyl)-4-[2-(2-methoxy-5-nitrophenyl)-1-(4-methoxyphenyl)ethyl-1,3-thiazol-2-amine; Step A; NaHMDS (30.0 mL, 30.0 mmol) was added to a -70C solution of ethyl 4-methoxyphenyl acetate (5.83 g, 30.0 mmol) and <strong>[3913-23-3]2-methoxy-5-nitrobenzyl bromide</strong> (7.38 g, 30.0 mmol) in 200 mL of THF. The reaction mixture was stirred to rt over a period of 16 h after which time the solvent was evaporated and the residue partitioned between 150 mL of EtOAc and 20 mL of saturated ammonium chloride. The aqueous phase was washed 2 x 25 mL of EtOAc and the combined organic extracts were washed with brine (20 mL) and dried over MgS04. The organic phase was dried, concentrated and chromatographed (0-50% EtOAc/hexane) to afford the monoalkylated target.
  • 2
  • [ 14062-18-1 ]
  • [ 1446332-69-9 ]
  • C25H28N2O5 [ No CAS ]
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