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[ CAS No. 52509-14-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 52509-14-5
Chemical Structure| 52509-14-5
Structure of 52509-14-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 52509-14-5 ]

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Product Details of [ 52509-14-5 ]

CAS No. :52509-14-5 MDL No. :MFCD00011966
Formula : C22H22BrO2P Boiling Point : -
Linear Structure Formula :- InChI Key :FRHRVQQUICVJDG-UHFFFAOYSA-M
M.W : 429.29 Pubchem ID :2724194
Synonyms :

Calculated chemistry of [ 52509-14-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 26
Num. arom. heavy atoms : 18
Fraction Csp3 : 0.18
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 114.42
TPSA : 32.05 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.2 cm/s

Lipophilicity

Log Po/w (iLOGP) : -1.09
Log Po/w (XLOGP3) : 5.24
Log Po/w (WLOGP) : 0.36
Log Po/w (MLOGP) : 4.4
Log Po/w (SILICOS-IT) : 4.74
Consensus Log Po/w : 2.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -5.99
Solubility : 0.000444 mg/ml ; 0.00000103 mol/l
Class : Moderately soluble
Log S (Ali) : -5.66
Solubility : 0.000935 mg/ml ; 0.00000218 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -7.99
Solubility : 0.00000438 mg/ml ; 0.0000000102 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 4.82

Safety of [ 52509-14-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 52509-14-5 ]

* 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 [ 52509-14-5 ]

[ 52509-14-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 4363-94-4 ]
  • [ 52509-14-5 ]
  • 4-((Z)-2-[1,3]Dioxolan-2-yl-vinyl)-6-methoxy-quinoline [ No CAS ]
  • 2
  • [ 52509-14-5 ]
  • [ 127406-08-0 ]
  • [ 868856-13-7 ]
YieldReaction ConditionsOperation in experiment
With Tris(3,6-dioxaheptyl)amine; potassium carbonate; In dichloromethane; water; for 17h;Heating / reflux; The compound from step A (6.2 g, 33.5 mmole), (1,3-dioxolan-2-yl-methyl)triphenylphosphonium bromide (22.6 g, 52.7 mmole), tris[2-(2-methoxyethoxy)ethyl]amine (11.2 ml, 34.9 mmole), sat. aq. K2CO3 (150 mls), and CH2Cl2 (150 ml) were heated at reflux for 17 hours. The mixture was cooled and the aqueous layer was washed with CH2Cl2 (2×). The combined organic layers were washed with NaHCO3, brine, dried (MgSO4), and concentrated.
  • 3
  • [ 40359-32-8 ]
  • [ 52509-14-5 ]
  • (E)-3-(3-(allyloxy)phenyl)acrylaldehyde [ No CAS ]
  • 4
  • [ 52509-14-5 ]
  • [ 24372-46-1 ]
  • (E)-3-(5-(dimethylamino)thiophen-2-yl)acrylaldehyde [ No CAS ]
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