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[ CAS No. 4518-10-9 ] {[proInfo.proName]}

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Chemical Structure| 4518-10-9
Chemical Structure| 4518-10-9
Structure of 4518-10-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4518-10-9 ]

CAS No. :4518-10-9 MDL No. :MFCD00017102
Formula : C8H9NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VZDNXXPBYLGWOS-UHFFFAOYSA-N
M.W : 151.16 Pubchem ID :78274
Synonyms :

Calculated chemistry of [ 4518-10-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.13
TPSA : 52.32 ?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) : -6.13 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.58
Log Po/w (XLOGP3) : 1.54
Log Po/w (WLOGP) : 1.06
Log Po/w (MLOGP) : 1.32
Log Po/w (SILICOS-IT) : 0.97
Consensus Log Po/w : 1.29

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.02
Solubility : 1.45 mg/ml ; 0.00957 mol/l
Class : Soluble
Log S (Ali) : -2.25
Solubility : 0.854 mg/ml ; 0.00565 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.1
Solubility : 1.21 mg/ml ; 0.008 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.11

Safety of [ 4518-10-9 ]

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

Application In Synthesis of [ 4518-10-9 ]

* 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.

  • Upstream synthesis route of [ 4518-10-9 ]
  • Downstream synthetic route of [ 4518-10-9 ]

[ 4518-10-9 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 4518-10-9 ]
  • [ 67-64-1 ]
  • [ 184150-96-7 ]
YieldReaction ConditionsOperation in experiment
83% With palladium diacetate; copper(II) acetate monohydrate In dimethyl sulfoxide at 80℃; for 48 h; Sealed tube; Inert atmosphere prepared a degass ed mixture of compound LVI (10.0 g, 0.061 mol) and copper(II) acetate 10 monohydrate (36.2 g, 0.182 mol) in dimethyls ulfoxide (50 mL). To the flask was added acetone (100 mL), followed by palladium(II) acetate (0.270 g, 0.001 mol), and the resulting reaction mixture was heated at 80 °C for 48 h. After cooling to room temperature, the reaction mixture was filtered through a pad of celite and the filtrate w as diluted with water (80 mL). The aqueous mixture w as extracted with ethyl acetate (3 x 100 mL) and the 148 of 363 {//-- DRAFT --//4069/3020WO/00228726/v2} 4069.3020 WO combined organic extracts were dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to obtain the crude product mixture, which was purified by silica gel chromatography using a gradient of 5-7percent ethyl acetate in hexanes as the eluant to affod LVII (4.8 g, 83percent) as a pale yellow solid.1H NMR (400 MHz, CDCl3) δ 8.26 (brs, 5 1H), 8.04 (s, 1H), 7.77 (dd, J= 8.3, 3.4 Hz, 1H), 7.50 (d, J= 8.3 Hz, 1H), 6.26 (s, 1H), 3.92 (s, 3H), 2.47 (s, 3H); MS (ESI, positive mode) m/z 190 (MH+).
Reference: [1] Patent: WO2015/73528, 2015, A1, . Location in patent: Page/Page column 148-149
  • 2
  • [ 4518-10-9 ]
  • [ 209459-11-0 ]
Reference: [1] Patent: WO2009/104155, 2009, A1,
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