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[ CAS No. 643-93-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 643-93-6
Chemical Structure| 643-93-6
Structure of 643-93-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 643-93-6 ]

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Product Details of [ 643-93-6 ]

CAS No. :643-93-6 MDL No. :MFCD00008533
Formula : C13H12 Boiling Point : -
Linear Structure Formula :- InChI Key :NPDIDUXTRAITDE-UHFFFAOYSA-N
M.W : 168.23 Pubchem ID :12564
Synonyms :

Calculated chemistry of [ 643-93-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.08
Num. rotatable bonds : 1
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 56.84
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.08 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.51
Log Po/w (XLOGP3) : 4.57
Log Po/w (WLOGP) : 3.66
Log Po/w (MLOGP) : 5.06
Log Po/w (SILICOS-IT) : 4.08
Consensus Log Po/w : 3.98

Druglikeness

Lipinski : 1.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.38
Solubility : 0.00703 mg/ml ; 0.0000418 mol/l
Class : Moderately soluble
Log S (Ali) : -4.29
Solubility : 0.00856 mg/ml ; 0.0000509 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.29
Solubility : 0.000855 mg/ml ; 0.00000508 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.3

Safety of [ 643-93-6 ]

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 [ 643-93-6 ]

* 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 [ 643-93-6 ]

[ 643-93-6 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 643-93-6 ]
  • [ 14704-31-5 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; Example 56 A mixture of 3-methylbiphenyl (5.23 g, 31.1 mmol), N-bromosuccinimide (5.56 g, 31.2 mmol), benzoyl peroxide (135 mg, 0.56 mmol), and carbon tetrachloride (150 ml) is refluxed for 17 h. The mixture is concentrated in vacuo and the residue is purified by flash column chromatography (hexane) to give 3-phenylbenzyl bromide.
  • 5
  • [ 13061-96-6 ]
  • [ 2113-58-8 ]
  • [ 643-93-6 ]
  • 6
  • [ 823-96-1 ]
  • [ 2113-58-8 ]
  • [ 643-93-6 ]
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