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[ CAS No. 1137826-05-1 ] {[proInfo.proName]}

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Chemical Structure| 1137826-05-1
Chemical Structure| 1137826-05-1
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Product Details of [ 1137826-05-1 ]

CAS No. :1137826-05-1 MDL No. :MFCD18417138
Formula : C10H7NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OKIIDYYKVMNMGL-UHFFFAOYSA-N
M.W : 189.17 Pubchem ID :58902455
Synonyms :

Calculated chemistry of [ 1137826-05-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 50.73
TPSA : 70.42 ?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) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.93
Log Po/w (XLOGP3) : 1.35
Log Po/w (WLOGP) : 1.64
Log Po/w (MLOGP) : -0.35
Log Po/w (SILICOS-IT) : 1.31
Consensus Log Po/w : 0.98

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.33
Solubility : 0.893 mg/ml ; 0.00472 mol/l
Class : Soluble
Log S (Ali) : -2.43
Solubility : 0.701 mg/ml ; 0.00371 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.5
Solubility : 0.597 mg/ml ; 0.00316 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.13

Safety of [ 1137826-05-1 ]

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

Application In Synthesis of [ 1137826-05-1 ]

* 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 [ 1137826-05-1 ]
  • Downstream synthetic route of [ 1137826-05-1 ]

[ 1137826-05-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 71082-47-8 ]
  • [ 1137826-05-1 ]
YieldReaction ConditionsOperation in experiment
91% With hydrogen bromide; acetic acid In water at 140℃; for 1 h; Microwave irradiation Example 11: N-hydroxy-6-phenoxyquinoline-3-carboxamide Compound 1-12 Step 1: 6-hydi*oxyquinoline-3-carboxylic acid Intermediate-15 [00183] 6-Methoxyquinoline-3-carbox lic acid (0.75 g, 3.69 mmol) was placed in a 20 mL microwave vial fitted with a stirbar. The solid was suspended in acetic acid (7 mL) and hydrobrorrric acid (48 percent in water, 3.5 mL) was added. The vial was capped and the suspension was carefully heated under microwave irradiation at 140 °C for 1 h. After reaction, the vial was thoroughly cooled to room temperature and very carefully vented with an 18 g needle in a fume hood prior to opening. The solids were collected by filtration and washed with ethyl acetate to afford the title product as a solid (0.678 g, 91 percent). LC-MS: (FA) ES+ 190; .H NMR (400 MHz, d6-DMSO) δ ppm 10.68 (br s, 1 H), 9.26 (d, J = 1.9 Hz, 1 H), 9.14 (d, J = 1.3 Hz, 1 H), 8.08 (d, J = 9.1 Hz, 1 H), 7,62 (dd, J = 9.1, 2.7 Hz, 1 H), 7.52 (d, J = 2.7 Hz, 1 H).
Reference: [1] Patent: WO2011/146591, 2011, A1, . Location in patent: Page/Page column 69
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