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[ CAS No. 149507-26-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 149507-26-6
Chemical Structure| 149507-26-6
Structure of 149507-26-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 149507-26-6 ]

CAS No. :149507-26-6 MDL No. :MFCD00807404
Formula : C7H8BFO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :IILGLPAJXQMKGQ-UHFFFAOYSA-N
M.W : 169.95 Pubchem ID :2782194
Synonyms :

Calculated chemistry of [ 149507-26-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 42.72
TPSA : 49.69 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.9
Log Po/w (WLOGP) : -0.07
Log Po/w (MLOGP) : 0.43
Log Po/w (SILICOS-IT) : -0.32
Consensus Log Po/w : 0.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.7
Solubility : 3.4 mg/ml ; 0.02 mol/l
Class : Very soluble
Log S (Ali) : -1.53
Solubility : 5.03 mg/ml ; 0.0296 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.69
Solubility : 3.48 mg/ml ; 0.0205 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.9

Safety of [ 149507-26-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 149507-26-6 ]

* 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 [ 149507-26-6 ]

[ 149507-26-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1445-39-2 ]
  • [ 149507-26-6 ]
  • [ 890021-33-7 ]
YieldReaction ConditionsOperation in experiment
Example 38; 5-(4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-N- phenylpyrimidin-2-amine; Step 1: Preparation of 5- (3-fluoro-4-methoxgammaphengammal) pyrimidin-2- amine; In a 500 mL round bottom flask under N2, 3-fluoro-4- methoxyphenylboronic acid (5.0 g, 29.4 mmol) and 5-iodopyrimidin- 2-amine (5.5 g, 24.9 mmol) were mixed. Toluene (100 mL) , EtOH (40 mL) and H2O (20 mL) were added, followed by the addition of Na2CO3 (3.0 g, 24.2 mmol). A stream of N2 was bubbled through the mixture for 5 min before the catalyst Pd(PPh)4 (0.30 g, 0.26 mmol) was added. The mixture was heated at 80 C under N2 for 20 h whereby it was cooled to RT. A solution of NaOH (5 N, 10 mL) was added to the mixture and stirring was continued for 10 min. The mixture was filtered and the solid was washed with H2O (3 x 10 mL) , followed by a mixture of hexanes - EtOAc (1:1, 30 mL) . The solid was dried in the air to give the title compound. MS (ESI pos. ion) m/z: 220. CaIc'd for C11H10FN3O: 219.08.
  • 2
  • [ 55305-43-6 ]
  • [ 149507-26-6 ]
  • [ 331-62-4 ]
  • 3
  • [ 261953-36-0 ]
  • [ 149507-26-6 ]
  • 6-(3-fluoro-4-methoxyphenyl)-1H-indazole [ No CAS ]
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