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[ CAS No. 14062-25-0 ] {[proInfo.proName]}

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Chemical Structure| 14062-25-0
Chemical Structure| 14062-25-0
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Product Details of [ 14062-25-0 ]

CAS No. :14062-25-0 MDL No. :MFCD00016333
Formula : C10H11BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ZFDCWHPNBWPPHG-UHFFFAOYSA-N
M.W : 243.10 Pubchem ID :7020609
Synonyms :

Calculated chemistry of [ 14062-25-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.81
TPSA : 26.3 ?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) : -5.67 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.73
Log Po/w (XLOGP3) : 2.97
Log Po/w (WLOGP) : 2.55
Log Po/w (MLOGP) : 2.99
Log Po/w (SILICOS-IT) : 3.06
Consensus Log Po/w : 2.86

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.3
Solubility : 0.123 mg/ml ; 0.000506 mol/l
Class : Soluble
Log S (Ali) : -3.19
Solubility : 0.159 mg/ml ; 0.000652 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.14
Solubility : 0.0175 mg/ml ; 0.0000721 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.7

Safety of [ 14062-25-0 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H302-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 14062-25-0 ]

* 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.

  • Upstream synthesis route of [ 14062-25-0 ]
  • Downstream synthetic route of [ 14062-25-0 ]

[ 14062-25-0 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 14062-25-0 ]
  • [ 1227159-85-4 ]
Reference: [1] Patent: US2011/301122, 2011, A1,
[2] Patent: US2013/196964, 2013, A1,
  • 2
  • [ 14062-25-0 ]
  • [ 1215205-50-7 ]
YieldReaction ConditionsOperation in experiment
85% With 1,8-diazabicyclo[5.4.0]undec-7-ene In dimethyl sulfoxide at 21℃; for 12 h; General procedure: To a 5 mL Schlenk tube were added aryl / heteroaryl acetates 3 (1.0 mmol, 1.0 equiv.), vinyl diphenylsulfonium triflate (434.4 mg, 1.2 mmol, 1.2 equiv.) and DMSO (5 mL). The mixture was stirred at room temperature for 2 min and to the mixture was added DBU (456 mg, 3 mmol, 3.0 equiv.). The mixture was stirred for 12 hours at room temperature till the reaction was complete. To the resulting mixture was added saturated ammonium chloride solution (25 mL), and the mixture was then extracted with EtOAc (3 x 150 mL). The combined organic layers were washed with H2O (2 x 30 mL), dried with anhydrous sodium sulfate. After concentration, product 4 was purified using column chromatography on silica gel using an appropriate eluent.
Reference: [1] Tetrahedron Letters, 2018, vol. 59, # 14, p. 1443 - 1445
  • 3
  • [ 14062-25-0 ]
  • [ 106-93-4 ]
  • [ 1215205-50-7 ]
YieldReaction ConditionsOperation in experiment
26% With sodium hydride In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil at 20℃; Example 14A
Ethyl 1-(4-bromophenyl)cyclopropanecarboxylate
1.45 g (36.2 mmol) of sodium hydride in mineral oil (60percent pure) were initially charged in 100 ml of DMF. A mixture of 4.0 g (16.5 mmol) of ethyl (4-bromophenyl)acetate and 6.5 g (34.6 mmol) of 1,2-dibromoethane was dissolved in 50 ml of THF and slowly added dropwise.
The mixture was stirred at RT overnight.
The reaction mixture was diluted with ethyl acetate and washed with water and saturated sodium chloride solution.
The organic phase was separated off, dried over magnesium sulphate and filtered, and the filtrate was concentrated.
The residue was purified by preparative HPLC [Reprosil C18, 10 μm, 250 mm*40 mm (30percent methanol/70percent water to 100percent methanol) over a run time of 25 min].
After HPLC control, the product-containing fractions were combined and concentrated.
This gave 1.15 g (26percent of theory) of a liquid.
GC-MS [Method 5]: Rt=5.45 min; MS(ESIpos): m/z=268/270 (M+)
1H-NMR (400 MHz, DMSO-d6): δ [ppm]=1.09 (t, 3H), 1.16-1.20 (m, 2H), 1.46-1.50 (m, 2H), 4.02 (q, 2H), 7.26-7.31 (m, 2H), 7.47-7.51 (m, 2H)
Reference: [1] Patent: US2016/318866, 2016, A1, . Location in patent: Paragraph 0642; 0643; 06444; 0645
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