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[ CAS No. 207742-88-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 207742-88-9
Chemical Structure| 207742-88-9
Structure of 207742-88-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 207742-88-9 ]

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Product Citations

Product Details of [ 207742-88-9 ]

CAS No. :207742-88-9 MDL No. :MFCD00149124
Formula : C7H8O5 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OSEOMYNJYKADOS-UHFFFAOYSA-N
M.W : 172.14 Pubchem ID :16211737
Synonyms :

Calculated chemistry of [ 207742-88-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 4.0
Molar Refractivity : 40.95
TPSA : 86.99 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -7.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.12
Log Po/w (XLOGP3) : 0.16
Log Po/w (WLOGP) : 0.55
Log Po/w (MLOGP) : -1.24
Log Po/w (SILICOS-IT) : 0.55
Consensus Log Po/w : 0.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.31
Solubility : 8.39 mg/ml ; 0.0487 mol/l
Class : Very soluble
Log S (Ali) : -1.54
Solubility : 4.92 mg/ml ; 0.0286 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.6
Solubility : 42.7 mg/ml ; 0.248 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.1

Safety of [ 207742-88-9 ]

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

Application In Synthesis of [ 207742-88-9 ]

* 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 [ 207742-88-9 ]

[ 207742-88-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 207742-88-9 ]
  • [ 51-78-5 ]
  • [ 1448846-11-4 ]
  • 2
  • [ 207742-88-9 ]
  • C57H87NO4 [ No CAS ]
  • 3
  • [ 207742-88-9 ]
  • (E)-2-(4′-hydroxybiphenyl-4-yl)-3-(3,4,5-tris-(dodecyloxy)phenyl)acrylonitrile [ No CAS ]
  • 4
  • [ 207742-88-9 ]
  • [ 143-15-7 ]
  • [ 117241-32-4 ]
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Technical Information

? Acidity of Phenols ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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