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[ CAS No. 849061-98-9 ] {[proInfo.proName]}

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Chemical Structure| 849061-98-9
Chemical Structure| 849061-98-9
Structure of 849061-98-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 849061-98-9 ]

CAS No. :849061-98-9 MDL No. :MFCD07369725
Formula : C7H6BFO3 Boiling Point : -
Linear Structure Formula :- InChI Key :YJXJCPZHXDDRNH-UHFFFAOYSA-N
M.W : 167.93 Pubchem ID :16217829
Synonyms :

Calculated chemistry of [ 849061-98-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 41.61
TPSA : 57.53 ?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) : -7.05 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.39
Log Po/w (WLOGP) : -0.26
Log Po/w (MLOGP) : 0.08
Log Po/w (SILICOS-IT) : -0.16
Consensus Log Po/w : 0.01

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.36
Solubility : 7.25 mg/ml ; 0.0432 mol/l
Class : Very soluble
Log S (Ali) : -1.16
Solubility : 11.5 mg/ml ; 0.0685 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.51
Solubility : 5.2 mg/ml ; 0.031 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.78

Safety of [ 849061-98-9 ]

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

Application In Synthesis of [ 849061-98-9 ]

* 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 [ 849061-98-9 ]

[ 849061-98-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 849061-98-9 ]
  • [ 84539-22-0 ]
  • 2-fluoro-3-[2-(morpholin-4-yl)pyrimidin-5-yl]benzaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
99% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,2-dimethoxyethane; water; at 80℃; for 2.5h;Inert atmosphere; General procedure: To a solution of <strong>[84539-22-0]4-(5-bromopyrimidin-2-yl)morpholine</strong> (17;4.10 g, 16.8 mmol) and ethyl [3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate (6.34 g, 21.8 mmol) in DME(82 mL)/H2O (41 mL) were added Na2CO3 (5.34 g, 50.4 mmol),and Pd(PPh3)4 (1.94 g, 1.68 mmol) under an argon atmosphere.The mixture was stirred at 80 C for 2.5 h. After being cooled toroom temperature, the mixture was diluted with H2O and EtOAc.The mixture was filtered, and the filtrate was separated. Theorganic layer was washed with H2O and brine, dried over Na2SO4,and concentrated in vacuo. The residue was purified by columnchromatography on silica gel (hexane/EtOAc = 17:3 to 3:2) and columnchromatography on amino functionalized silica gel (hexane/EtOAc = 9:1 to 7:3) to give the product (5.29 g, 96%) as a colorlesssolid. 1H NMR (DMSO-d6): d 1.19 (3H, t, J = 7.1 Hz), 3.64-3.79 (8H,m), 3.72 (2H, s), 4.10 (2H, q, J = 7.1 Hz), 7.25 (1H, d, J = 7.6 Hz),7.35-7.45 (1H, m), 7.50-7.58 (2H, m), 8.70 (2H, s); MS (ESI) m/z[M+H]+ 328.
  • 2
  • [ 849061-98-9 ]
  • [ 2923-66-2 ]
  • [ 19335-11-6 ]
  • (3-(9-(3-chloro-4-fluorophenyl)-3H-pyrazolo[4,3-f]quinolin-7-yl)-2-fluorophenyl)boronic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
15% General procedure: Amine (1 mmol) and aldehyde (1 mmol) in 5 mL of absolute ethanol refluxed for 2 h. After that,ketone (2.5 mmol) and catalytic amount of conc. hydrochloric acid was added to the reaction mixture. The reaction mixture was continued to reflux for another 6-12 h. After completion, thereaction mixture was concentrated and purified by silica gel chromatography (Hexanes/ethylacetate 95:5 to 50:50) or dichloromethane/methanol (99:01 to 80:20) to give the desired cyclized compound.
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