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[ CAS No. 4255-62-3 ] {[proInfo.proName]}

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Chemical Structure| 4255-62-3
Chemical Structure| 4255-62-3
Structure of 4255-62-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4255-62-3 ]

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Product Details of [ 4255-62-3 ]

CAS No. :4255-62-3 MDL No. :MFCD00234965
Formula : C8H14O Boiling Point : -
Linear Structure Formula :(CH3)2C6H8O InChI Key :PXQMSTLNSHMSJB-UHFFFAOYSA-N
M.W : 126.20 Pubchem ID :138166
Synonyms :

Calculated chemistry of [ 4255-62-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.4
TPSA : 17.07 ?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) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.89
Log Po/w (XLOGP3) : 1.58
Log Po/w (WLOGP) : 2.16
Log Po/w (MLOGP) : 1.68
Log Po/w (SILICOS-IT) : 2.55
Consensus Log Po/w : 1.97

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.62
Solubility : 3.04 mg/ml ; 0.0241 mol/l
Class : Very soluble
Log S (Ali) : -1.55
Solubility : 3.56 mg/ml ; 0.0282 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.16
Solubility : 0.879 mg/ml ; 0.00697 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.51

Safety of [ 4255-62-3 ]

Signal Word:Danger Class:4.1
Precautionary Statements:P264-P210-P240-P280-P305+P351+P338-P337+P313-P370+P378-P403+P233-P501 UN#:1325
Hazard Statements:H228-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4255-62-3 ]

* 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 [ 4255-62-3 ]

[ 4255-62-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 34270-90-1 ]
  • [ 4255-62-3 ]
  • [ 97827-52-6 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride; In tetrahydrofuran; at 65℃; for 2h;Reflux; Step 1 :NaH (60% in oil, 975 mg, 24.38 mmol) is washed with pentane (3x) and then suspended in dry THF (10 mL). A solution of 4,4-dimethyl cyclohexanone (1.02 g, 8.12 mmol, Combi-Blocks) in THF (5 mL) is added, followed by bis-2-iodoethyl ether (1.25 mL, 8.80 mmol). The reaction mixture is heated to 65C. When an exothermic reaction occurs, external heating is stopped and the reaction mixture is stirred for 1.5 h. The reaction mixture is heated at reflux for 30 min, and then is poured into water and extracted with ether. The aqueous phase is acidified to pH 6 with 1 M HCI and extracted with ether (2x). The filtrate is dried over anhydrous Na2S04, concentrated under reduced pressure and purified by Combiflash (90:10Hex EtOAc) to afford 6a1.
  • 2
  • [ 50-00-0 ]
  • [ 187669-28-9 ]
  • [ 4255-62-3 ]
  • [ 1044598-92-6 ]
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