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[ CAS No. 14140-15-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 14140-15-9
Chemical Structure| 14140-15-9
Structure of 14140-15-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 14140-15-9 ]

CAS No. :14140-15-9 MDL No. :MFCD00129679
Formula : C8H9BrO Boiling Point : -
Linear Structure Formula :- InChI Key :DYYVTFCYVZEQDG-UHFFFAOYSA-N
M.W : 201.06 Pubchem ID :84221
Synonyms :
Chemical Name :4-(2-Bromoethyl)phenol

Calculated chemistry of [ 14140-15-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 2
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.11
TPSA : 20.23 ?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) : -5.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 2.8
Log Po/w (WLOGP) : 2.33
Log Po/w (MLOGP) : 2.61
Log Po/w (SILICOS-IT) : 2.68
Consensus Log Po/w : 2.47

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.16
Solubility : 0.138 mg/ml ; 0.000688 mol/l
Class : Soluble
Log S (Ali) : -2.88
Solubility : 0.264 mg/ml ; 0.00131 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.49
Solubility : 0.0652 mg/ml ; 0.000324 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.39

Safety of [ 14140-15-9 ]

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 [ 14140-15-9 ]

* 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 [ 14140-15-9 ]

[ 14140-15-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 14140-15-9 ]
  • [ 124-40-3 ]
  • [ 539-15-1 ]
YieldReaction ConditionsOperation in experiment
92% In methanol; at 20℃; To 250 mg of 4-hydroxyphenethyl bromide in a round-bottomed flask, a 10 M excess of methylamine (6.22 mL of 2M in MeOH) was added and the solution was stirred at r.t. overnight. After filtration, the solvent was evaporated and gave the product in crystalline form in 92% yield, 0.23 g, light yellow, m.p.: 73-76 0C. TLC (EtAc:MeOH, 9:1 v/v): RF = 0.1. H NMR, delta: 9.43 (s, 1 H), 7.12 (d, 2H), 6.70 (d, 2 H), 2.74 (m, 4H), 2.30 (s, 6 H). 3C NMR, delta: 167.5, 134.3, 130.2, 115.6, 60.6, 45.9, 32.4. Anal, calcd for C10H15NO: C, 72.69; H, 9.15; N, 8.48%. Found; C, 72.60; H, 9.30; N, 8.40%.
  • 2
  • [ 14140-15-9 ]
  • [ 102831-44-7 ]
  • [ 1239577-86-6 ]
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