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[ CAS No. 22236-08-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 22236-08-4
Chemical Structure| 22236-08-4
Structure of 22236-08-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 22236-08-4 ]

CAS No. :22236-08-4 MDL No. :MFCD00236221
Formula : C7H7F2NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :RSOFZRXRIPVBBM-UHFFFAOYSA-N
M.W : 159.13 Pubchem ID :2774110
Synonyms :

Calculated chemistry of [ 22236-08-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 37.44
TPSA : 35.25 ?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) : -5.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.41
Log Po/w (XLOGP3) : 1.88
Log Po/w (WLOGP) : 2.72
Log Po/w (MLOGP) : 1.48
Log Po/w (SILICOS-IT) : 1.51
Consensus Log Po/w : 1.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.28
Solubility : 0.83 mg/ml ; 0.00522 mol/l
Class : Soluble
Log S (Ali) : -2.24
Solubility : 0.911 mg/ml ; 0.00572 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.37
Solubility : 0.674 mg/ml ; 0.00424 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.47

Safety of [ 22236-08-4 ]

Signal Word:Warning Class:
Precautionary Statements:P210-P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P370+P378-P403+P235-P501 UN#:
Hazard Statements:H227-H302+H312+H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 22236-08-4 ]

* 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 [ 22236-08-4 ]

[ 22236-08-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22236-08-4 ]
  • [ 402-69-7 ]
  • N-(3-(difluoromethoxy)phenyl)-6-fluoro-2-picolinamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
55.9% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 20 - 50℃; General procedure: The synthesis was carried out by using the synthetic method a. To a solution of 2-picolinic acid (0.871 g,7.08 mmol), N-hydroxybenzotriazolehydrate (HOBt.H2O,1.084 g, 7.08 mmol), diisopropylethylamine(DIPEA, 1.83 g, 14.17mmol) and N-(3-methylaminopropyl)-N?-ethylcarbodiimidehydrochloride (EDCHCl, 2.036 g, 10.63mmol) in anhydrous 1,4-dioxane (60 mL) was added 3-fluoro-3-methoxyanilline (1.00 g, 7.08 mmol) at room temperature. The mixture was heated to 50 oC and stirred overnight. To the reaction mixture was added 300 mL of dichloromethane, and sequentially washed with water (3 x100 mL). After the organic layer was separated and concentrated, the reaction mixture was purified by silica-gel chromatography (hexane/ethyl acetate) to give the product as a pale-yellow solid (1.559 g, 6.33mmol, 89.4percent yield).
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