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[ CAS No. 1009735-24-3 ] {[proInfo.proName]}

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Chemical Structure| 1009735-24-3
Chemical Structure| 1009735-24-3
Structure of 1009735-24-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1009735-24-3 ]

CAS No. :1009735-24-3 MDL No. :MFCD18257518
Formula : C8H8BrNO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BPQKMODYCOBBPO-UHFFFAOYSA-N
M.W : 246.06 Pubchem ID :71721354
Synonyms :

Calculated chemistry of [ 1009735-24-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.71
TPSA : 48.42 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.36 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.5
Log Po/w (XLOGP3) : 2.03
Log Po/w (WLOGP) : 1.64
Log Po/w (MLOGP) : 1.22
Log Po/w (SILICOS-IT) : 1.89
Consensus Log Po/w : 1.85

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.79
Solubility : 0.401 mg/ml ; 0.00163 mol/l
Class : Soluble
Log S (Ali) : -2.67
Solubility : 0.521 mg/ml ; 0.00212 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.09
Solubility : 0.201 mg/ml ; 0.000818 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.03

Safety of [ 1009735-24-3 ]

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

Application In Synthesis of [ 1009735-24-3 ]

* 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 [ 1009735-24-3 ]

[ 1009735-24-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1060806-62-3 ]
  • [ 74-88-4 ]
  • [ 1009735-24-3 ]
YieldReaction ConditionsOperation in experiment
40% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 16h; Step 2: <strong>[1060806-62-3]6-bromo-2-methoxy-nicotinic acid</strong> methyl ester; To potassium carbonate (1.34 g, 9.48 mmol) in N,N-dimethylformamide (10 mL) was added <strong>[1060806-62-3]6-bromo-2-methoxy-nicotinic acid</strong> (1.10 g, 4.74 mmol) and methyl iodide (0.895 g, 6.31 mmol). The reaction was stirred for 16 h at room temperature. The reaction mixture was diluted with water and ethyl acetate, the layers were separated. The aqueous layer was washed with ethyl acetate 2 times. The combined organic layers were washed with brine and dried over magnesium sulfate, filtered and concentrated. The filtrate was concentrated and purified by silica gel column chromatography eluting with a gradient of 5% - 10% ethyl acetate/ heptane to obtain the title compound as a colorless oil (0.459 g, 40%). 1 H NMR (500 MHz, DMSO-d6) delta ppm 3.81 (3 H, s), 3.93 (3 H, s), 7.36 (1 H, d, J=7.8 Hz), 8.06 (1 H, d, J=7.8 Hz).
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