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[ CAS No. 19962-06-2 ] {[proInfo.proName]}

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Chemical Structure| 19962-06-2
Chemical Structure| 19962-06-2
Structure of 19962-06-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 19962-06-2 ]

CAS No. :19962-06-2 MDL No. :MFCD06798070
Formula : C11H15NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :HJQNVUQTARSZDK-UHFFFAOYSA-N
M.W : 209.24 Pubchem ID :312485
Synonyms :

Calculated chemistry of [ 19962-06-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 58.71
TPSA : 58.56 ?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) : -6.07 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.15
Log Po/w (XLOGP3) : 2.12
Log Po/w (WLOGP) : 2.55
Log Po/w (MLOGP) : 1.79
Log Po/w (SILICOS-IT) : 1.19
Consensus Log Po/w : 1.96

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.5
Solubility : 0.654 mg/ml ; 0.00313 mol/l
Class : Soluble
Log S (Ali) : -2.98
Solubility : 0.219 mg/ml ; 0.00104 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.78
Solubility : 0.347 mg/ml ; 0.00166 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.06

Safety of [ 19962-06-2 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280 UN#:
Hazard Statements:H317 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 19962-06-2 ]

* 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 [ 19962-06-2 ]

[ 19962-06-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 19962-06-2 ]
  • [ 6627-22-1 ]
  • [ 827042-49-9 ]
YieldReaction ConditionsOperation in experiment
93% With caesium carbonate; In DMF (N,N-dimethyl-formamide); at 20℃; for 5h; 868 mg (4.763 MMOL) 6-CHLORO-PYRIMIDINE-4-CARBOXYLIC acid methyl ester are suspended in 10 ml of DMF together with 1 g (4.763 MMOL) (3- Hydroxy-phenyl)-carbamic acid, ter-butyl ester (S. J. Gould, R. L. Eisenberg, J. Org. Chem. 56 (23), 1991, 6666) and 1.54 g (4. 763 MMOL) cesium carbonate and stirred for 5 H at room temperature. The reaction mixture is poured onto ice and extracted several times with ethyl acetate. The combined organic phases are washed with water, dried over NA2SO4, filtered and evaporated. Yield : 1.58 g (93 %) brown oil
  • 2
  • [ 2106-49-2 ]
  • [ 19962-06-2 ]
  • (3-(2-chloro-4-nitrophenoxy)phenyl)carbamic acid tert-butyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
78.8% With potassium hydroxide; In acetonitrile; at 40℃; for 2h; Dissolve 3- (tert-butoxycarbonyl) aminophenol (1.05g, 5.0mmol) in acetonitrile (10mL), add KOH (351mg, 6.25mmol), stir to 40 C, and add 3-chloro-4-fluoronitro Benzene (878 mg, 5.0 mmol) was reacted at 40 C for 2 h. The starting material disappeared. It was concentrated, EA (25 mL) was added, and water (20 mL × 2) was extracted. The organic phase was combined with anhydrous magnesium sulfate and dried, and column chromatography (P / E = 40: 1) gave 1.437 g of a colorless oil with a yield of 78.8%.
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