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[ CAS No. 98447-30-4 ] {[proInfo.proName]}

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Chemical Structure| 98447-30-4
Chemical Structure| 98447-30-4
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Product Details of [ 98447-30-4 ]

CAS No. :98447-30-4 MDL No. :MFCD06797977
Formula : C7H6BrNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :RYKPDLZQIABTMY-UHFFFAOYSA-N
M.W : 232.03 Pubchem ID :12966745
Synonyms :

Calculated chemistry of [ 98447-30-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.46
TPSA : 55.05 ?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) : -5.81 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.77
Log Po/w (XLOGP3) : 2.68
Log Po/w (WLOGP) : 2.37
Log Po/w (MLOGP) : 2.18
Log Po/w (SILICOS-IT) : 0.35
Consensus Log Po/w : 1.87

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.2
Solubility : 0.145 mg/ml ; 0.000624 mol/l
Class : Soluble
Log S (Ali) : -3.49
Solubility : 0.0754 mg/ml ; 0.000325 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.77
Solubility : 0.399 mg/ml ; 0.00172 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.86

Safety of [ 98447-30-4 ]

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

Application In Synthesis of [ 98447-30-4 ]

* 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 [ 98447-30-4 ]

[ 98447-30-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 5470-65-5 ]
  • [ 77-78-1 ]
  • [ 98447-30-4 ]
  • 2
  • [ 5470-65-5 ]
  • [ 74-88-4 ]
  • [ 98447-30-4 ]
YieldReaction ConditionsOperation in experiment
85.0% With potassium carbonate; In diethyl ether; water; ethyl acetate; N,N-dimethyl-formamide; Example 2 2-Bromo-4-methoxy-1-nitrobenzene (Compound 5) Compound 4 (2.0 g, 9.22 mmol) was dissolved in DMF (40 mL), and K2CO3 (2.5 g, 18.44 mmol) was added. The reaction mixture was stirred at room temperature for 20 min. After cooling to 0° C., a solution of iodomethane (861 muL, 13.83 mmol) in DMF (5 mL) was added dropwise, and the resulting mixture was stirred at room temperature for 2 h. The reaction was quenched by adding H2O (100 mL) and partitioned with Et2O (200 mL). The organic layer was washed with H2O (3*50 mL) and brine (50 mL). The organic layer was collected, dried over anhydrous Na2SO4, filtered, concentrated, and purified by silica column chromatography (20percent EtOAc in hexanes) to afford compound 5 in 85.0percent (1.81 g) yield as a yellow solid. 1H-NMR (CDCl3, 400 MHz) delta 7.89 (1H, d, J=9.2 Hz, Ar), 7.22 (1H, s, Ar), 6.91 (1H, d, J=9.2 Hz, Ar), 3.89 (3H, s, OCH3); MS (ESI) m/z Calcd for C7H6BrNO3 (M+): 231.0, Found: 232.1 (M+H+).
  • 3
  • [ 98447-30-4 ]
  • [ 175883-62-2 ]
  • [ 29093-41-2 ]
  • 2,6-dimethoxy-1-methyl-9H-carbazole [ No CAS ]
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