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[ CAS No. 57486-69-8 ] {[proInfo.proName]}

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Chemical Structure| 57486-69-8
Chemical Structure| 57486-69-8
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Product Details of [ 57486-69-8 ]

CAS No. :57486-69-8 MDL No. :MFCD07779430
Formula : C9H9BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 229.07 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 57486-69-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 50.01
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) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.41
Log Po/w (XLOGP3) : 2.4
Log Po/w (WLOGP) : 2.16
Log Po/w (MLOGP) : 2.7
Log Po/w (SILICOS-IT) : 2.71
Consensus Log Po/w : 2.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.94
Solubility : 0.26 mg/ml ; 0.00114 mol/l
Class : Soluble
Log S (Ali) : -2.59
Solubility : 0.583 mg/ml ; 0.00255 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.74
Solubility : 0.0419 mg/ml ; 0.000183 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 57486-69-8 ]

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 [ 57486-69-8 ]

* 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 [ 57486-69-8 ]

[ 57486-69-8 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 57486-69-8 ]
  • [ 4009-98-7 ]
  • [ 122394-38-1 ]
  • (E)-methyl 3-methoxy-2-[2-(3-methylphenoxy)phenyl]propenoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With selenium(IV) oxide; potassium tert-butylate; In hexane; EXAMPLE 3 This Example illustrates an alternative synthesis of (E)-methyl 3-methoxy-2-[2-(3-methylphenoxy)phenyl]propenoate. A mixture of methyl ortho-bromophenylacetate (4.10 g, prepared as described in Example 1) and selenium dioxide (4.92 g) was stirred for 25 hours at 190 C. After cooling, the mixture was diluted with dichloromethane (100 ml) then filtered through `Supercel`. The filtrate was washed successively with saturated aqueous sodium bicarbonate (*2) and brine, then dried and concentrated to give a yellow liquid (3.60 g) containing (52% by GC-MS) <strong>[122394-38-1]methyl (2-bromobenzoyl)formate</strong> and unreacted methyl ortho-bromophenylacetate. Potassium tert-butoxide (2.33 g) was added to a vigorously-stirred suspension of (methoxymethyl)triphenylphosphonium chloride (7.90 g) in ether (80 ml) at room temperature. After 15 minutes, a solution of the crude <strong>[122394-38-1]methyl (2-bromobenzoyl)formate</strong> (3.60 g) in ether (10 ml) was added in a single portion. After a further 15 minutes, the reaction mixture was poured into water (150 ml), the aqueous and organic layers were separated, and the former was extracted with a further portion of ether (100 ml). The combined ether layers were washed successively with water (*2) and brine, then dried and concentrated to give a yellow oil (5.81 g) containing, in a ratio of about 6:5, the (E)- and (Z)-isomers respectively of methyl 2-(2-bromophenyl)-3-methoxypropenoate. Chromatography using ether:hexane (1:1) as eluant allowed the pure (Z)-isomer (0.450 g) to be isolated as a pale yellow oil, IR (film) 1712, 1638 cm-1, 1 H n.m.r delta 3.71 (3H, s), 3.95 (3H, s), 6.57 (1H, s) p.p.m.
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