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[ CAS No. 54840-15-2 ] {[proInfo.proName]}

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Chemical Structure| 54840-15-2
Chemical Structure| 54840-15-2
Structure of 54840-15-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 54840-15-2 ]

CAS No. :54840-15-2 MDL No. :MFCD00226573
Formula : C11H15NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :YRQMBQUMJFVZLF-UHFFFAOYSA-N
M.W : 209.24 Pubchem ID :2756771
Synonyms :

Calculated chemistry of [ 54840-15-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 58.71
TPSA : 58.56 ?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) : -6.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.12
Log Po/w (XLOGP3) : 1.85
Log Po/w (WLOGP) : 2.55
Log Po/w (MLOGP) : 1.79
Log Po/w (SILICOS-IT) : 1.19
Consensus Log Po/w : 1.9

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.33
Solubility : 0.968 mg/ml ; 0.00463 mol/l
Class : Soluble
Log S (Ali) : -2.7
Solubility : 0.417 mg/ml ; 0.00199 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.78
Solubility : 0.347 mg/ml ; 0.00166 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.91

Safety of [ 54840-15-2 ]

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 [ 54840-15-2 ]

* 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 [ 54840-15-2 ]

[ 54840-15-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 207399-07-3 ]
  • [ 54840-15-2 ]
  • [ 1242439-55-9 ]
YieldReaction ConditionsOperation in experiment
73% Compound 4 (126 mg, 0.60 mmol) was dissolved in DMF (15 mL), the solution was added with sodium hydride (60% in oil, 24 mg, 0.60 mmol), and the mixture was stirred at room temperature for 10 minutes under an argon atmosphere. The reaction solution was added with <strong>[207399-07-3]<strong>[207399-07-3]IR-780</strong> iodide</strong> (200 mg, 0.30 mmol) dissolved in DMF (15 mL), and the mixture was further stirred at room temperature for 16 hours. After the solvent was evaporated, the residue was purified by silica gel column chromatography (NH silica, dichloromethane/methanol, 19:1) to obtain Compound 5 (184 mg, 73%) as green solid.1H-NMR (300 MHz, CDCl3): δ 1.05 (t, J=7.4 Hz, 6H), 1.36 (s, 12H), 1.50 (s, 9H), 1.87 (sex, J=7.4 Hz, 4H), 2.05 (t, J=5.5 Hz, 2H), 2.72 (t, J=5.5 Hz, 4H), 4.05 (t, J=7.4 Hz, 4H), 6.05 (d, J=14.3 Hz, 2H), 6.80 (br s, 1H), 6.99 (d, J=9.0 Hz, 2H), 7.09 (d, J=7.7 Hz, 2H), 7.20 (d, J=7.7 Hz, 2H), 7.27 (d, J=6.8 Hz, 2H), 7.34 (d, J=6.8 Hz, 2H), 7.47 (d, J'29.0 Hz, 2H), 7.91 (d, J=14.3 Hz, 2H)LRMS (ESI+): m/z 712 (M-I)+
  • 2
  • [ 54840-15-2 ]
  • [ 102877-78-1 ]
  • 3
  • [ 54840-15-2 ]
  • [ 7379-35-3 ]
  • [ 102877-78-1 ]
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