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[ CAS No. 2177-70-0 ] {[proInfo.proName]}

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Chemical Structure| 2177-70-0
Chemical Structure| 2177-70-0
Structure of 2177-70-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2177-70-0 ]

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Product Details of [ 2177-70-0 ]

CAS No. :2177-70-0 MDL No. :MFCD00048117
Formula : C10H10O2 Boiling Point : -
Linear Structure Formula :C6H5OCOC(CH3)CH2 InChI Key :QIWKUEJZZCOPFV-UHFFFAOYSA-N
M.W : 162.18 Pubchem ID :75121
Synonyms :

Calculated chemistry of [ 2177-70-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.1
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.08
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) : -5.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.28
Log Po/w (XLOGP3) : 2.64
Log Po/w (WLOGP) : 2.17
Log Po/w (MLOGP) : 2.47
Log Po/w (SILICOS-IT) : 2.22
Consensus Log Po/w : 2.35

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.68
Solubility : 0.338 mg/ml ; 0.00209 mol/l
Class : Soluble
Log S (Ali) : -2.84
Solubility : 0.233 mg/ml ; 0.00144 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.91
Solubility : 0.2 mg/ml ; 0.00123 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.54

Safety of [ 2177-70-0 ]

Signal Word:Danger Class:3
Precautionary Statements:P261-P305+P351+P338 UN#:3272
Hazard Statements:H225-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2177-70-0 ]

* 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.

  • Downstream synthetic route of [ 2177-70-0 ]

[ 2177-70-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 645-67-0 ]
  • [ 2177-70-0 ]
  • C15H18O4 [ No CAS ]
  • C15H18O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With copper(II) acetate hydrate; C43H39FeNP2; In toluene;Inert atmosphere; Under nitrogen protection,Taniaphos ligand L3 (R4=R5=Ph) (5.3 mg) was added to the dry reaction flask.Cu(OAc)2·H2O (3.0 mg), toluene (1.0 mL),Polymethylhydrogensiloxane (100μL),Stir thoroughly. To the above mixture, phenyl methacrylate (200 μL) was added dropwise with stirring.A solution of propyl 3- levulinate (128 mg) in toluene (4.0 mL),After the addition was complete, the reaction was stirred overnight. Saturated aqueous NH4F solution (2 mL) was added to the reaction mixture.After stirring for 30 min, the phases were separated and the aqueous phase was extracted with dichloromethane (3 x 5 mL).The combined organic phases are washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated.After column chromatography, γ-methyl-γ-(1-methyl-1-phenoxycarbonylethyl)-γ-cyclobutyrolactone (203 mg, yield 77%, ee value) was obtained as a colorless oily liquid. 16%).
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