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[ CAS No. 4415-82-1 ] {[proInfo.proName]}

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Chemical Structure| 4415-82-1
Chemical Structure| 4415-82-1
Structure of 4415-82-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4415-82-1 ]

CAS No. :4415-82-1 MDL No. :MFCD00001330
Formula : C5H10O Boiling Point : No data available
Linear Structure Formula :- InChI Key :WPOPOPFNZYPKAV-UHFFFAOYSA-N
M.W : 86.13 Pubchem ID :78130
Synonyms :

Calculated chemistry of [ 4415-82-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 25.2
TPSA : 20.23 ?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) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.63
Log Po/w (XLOGP3) : 0.83
Log Po/w (WLOGP) : 0.78
Log Po/w (MLOGP) : 0.76
Log Po/w (SILICOS-IT) : 1.27
Consensus Log Po/w : 1.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.83
Solubility : 12.7 mg/ml ; 0.148 mol/l
Class : Very soluble
Log S (Ali) : -0.84
Solubility : 12.5 mg/ml ; 0.145 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.48
Solubility : 28.4 mg/ml ; 0.33 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.17

Safety of [ 4415-82-1 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P403+P235 UN#:1987
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4415-82-1 ]

* 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 [ 4415-82-1 ]

[ 4415-82-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 28114-87-6 ]
  • [ 4415-82-1 ]
  • cyclobutylmethyl spiro[3.3]heptane-2-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
69.8% With toluene-4-sulfonic acid; In tetrahydrofuran; benzene; for 4.0h;Dean-Stark; Heating; 1.40 g (9.6 mmol) of Spiro [3,3] heptane-2-carboxylic acid and 1.00 g (11.50 mmol) of Cyclobutylmethanol and 1.88 g (9.6 mmol) ofParatoluenesulfonic acid was dissolved in 12 ml of benzene solution and 4 ml of tetrahydrofuran solution, and then a Dean-Stark trap was provided and stirred at 80 C. After 4 hours, the organic material was extracted with 15 ml of distilled water and 15 ml of ethyl ether. The organic extracts were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography (hexane: ethyl acetate = 50: 1) to obtain 1.4 g (6.7 mmol, spiro [3,3] heptane- : 69.8%) of the compound represented by the formula (8) was obtained.
  • 2
  • [ 4415-82-1 ]
  • [ 103962-05-6 ]
  • Cyclobutyl-[4-(trifluoromethoxy)phenyl]methanol [ No CAS ]
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