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[ CAS No. 78887-39-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 78887-39-5
Chemical Structure| 78887-39-5
Structure of 78887-39-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 78887-39-5 ]

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Product Citations

Product Details of [ 78887-39-5 ]

CAS No. :78887-39-5 MDL No. :MFCD00236013
Formula : C8H10BNO3 Boiling Point : -
Linear Structure Formula :B(OH)2C6H4NHCOCH3 InChI Key :IBTSWKLSEOGJGJ-UHFFFAOYSA-N
M.W : 178.98 Pubchem ID :157274
Synonyms :

Calculated chemistry of [ 78887-39-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 3.0
Molar Refractivity : 50.58
TPSA : 69.56 ?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) : -7.39 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.0
Log Po/w (WLOGP) : -0.87
Log Po/w (MLOGP) : -0.2
Log Po/w (SILICOS-IT) : -1.19
Consensus Log Po/w : -0.45

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.09
Solubility : 14.4 mg/ml ; 0.0807 mol/l
Class : Very soluble
Log S (Ali) : -1.01
Solubility : 17.4 mg/ml ; 0.0973 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.67
Solubility : 3.79 mg/ml ; 0.0212 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.68

Safety of [ 78887-39-5 ]

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

Application In Synthesis of [ 78887-39-5 ]

* 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 [ 78887-39-5 ]

[ 78887-39-5 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 13771-68-1 ]
  • [ 78887-39-5 ]
  • [ 907945-25-9 ]
YieldReaction ConditionsOperation in experiment
Ethyl 5-bromo-1-benzothiophene-2-carboxylate (2.0 g), 3-acetamidobenzene boronic acid (1.38 g), 1 M potassium carbonate aqueous solution (15 mL) and ethanol (15 mL) were added to toluene (50 mL), and stirred for 30 minutes at room temperature in an argon atmosphere. Tetrakis triphenylphosphine palladium (0.24 g) was added and refluxed for 8 hours. The mixture was extracted with ethyl acetate, the organic layer was washed with water and sodium chloride solution and dried over magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane) to obtain ethyl 5-[3-(acetylamino)phenyl]-1-benzothiophene-2-carboxylate (1.91 g) as pale brown crystals. 1H-NMR (300MHz, CDCl3) δ 1.43 (3H, t, J = 7.1 Hz), 2.22 (3H, s), 4.43 (2H, q, J = 7.1 Hz), 7.34-7.54 (3H, m), 7.69 (1H, dd, J = 1.7, 8.5 Hz), 7.85 (1H, s), 7.91 (1H, d, J = 8.5 Hz), 8.05 (1H, d, J = 1.7Hz), 8.09(1H, s)
  • 2
  • [ 78887-39-5 ]
  • [ 120-35-4 ]
  • 3-(3-Acetylamino-phenylamino)-4-methoxy-N-phenyl-benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 280 3-(3-Acetylamino-phenylamino)-4-methoxy-N-phenyl-benzamide The title compound has been made using the procedure of Example 154, but using <strong>[120-35-4]3-amino-4-methoxy-benzanilide</strong>, which is available from Aldrich, and 3-acetamidobenzeneboronic acid, which is available from Lancaster, as starting materials; mp 202-203 C.
  • 3
  • [ 76-09-5 ]
  • [ 78887-39-5 ]
  • [ 480424-93-9 ]
  • 4
  • [ 2296-23-3 ]
  • [ 78887-39-5 ]
  • [ 1386859-32-0 ]
  • 5
  • [ 2296-23-3 ]
  • [ 78887-39-5 ]
  • [ 1386859-24-0 ]
  • 6
  • [ 13675-18-8 ]
  • [ 621-38-5 ]
  • [ 78887-39-5 ]
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