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[ CAS No. 476-66-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 476-66-4
Chemical Structure| 476-66-4
Structure of 476-66-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 476-66-4 ]

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Product Details of [ 476-66-4 ]

CAS No. :476-66-4 MDL No. :MFCD00006914
Formula : C14H6O8 Boiling Point : -
Linear Structure Formula :- InChI Key :AFSDNFLWKVMVRB-UHFFFAOYSA-N
M.W : 302.19 Pubchem ID :5281855
Synonyms :
Gallogen;Elagostasine;HSDB 7574;CCRIS 774;Benzoaric acid;Alizarine Yellow;TBBD;Lagistase
Chemical Name :2,3,7,8-Tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione

Calculated chemistry of [ 476-66-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 22
Num. arom. heavy atoms : 16
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 8.0
Num. H-bond donors : 4.0
Molar Refractivity : 75.31
TPSA : 141.34 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.36 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.79
Log Po/w (XLOGP3) : 1.1
Log Po/w (WLOGP) : 1.31
Log Po/w (MLOGP) : 0.14
Log Po/w (SILICOS-IT) : 1.67
Consensus Log Po/w : 1.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.94
Solubility : 0.343 mg/ml ; 0.00114 mol/l
Class : Soluble
Log S (Ali) : -3.66
Solubility : 0.066 mg/ml ; 0.000218 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.35
Solubility : 0.136 mg/ml ; 0.000449 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 3.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.17

Safety of [ 476-66-4 ]

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 [ 476-66-4 ]

* 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 [ 476-66-4 ]

[ 476-66-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 618-73-5 ]
  • [ 476-66-4 ]
YieldReaction ConditionsOperation in experiment
84% With 3-chloro-benzenecarboperoxoic acid; for 10.0h; Weigh 50g of gallic acid,Pour into a 500ml jar after drying,Then added 25% concentrated ammonia water 250ml,Plug the bottle with a stopper,Stir in a constant temperature water bath at 50 C for 12 h.The reaction solution was then poured into a 1000 ml dry three-necked flask.60 g of m-CPBA was charged and reacted for 10 hours.After the reaction is over,Filter the reaction solution,The filter cake was dissolved in 10% NaOH solution.Put in 250g of activated carbon,Stirring at 35 C,Filtration, the filtrate was extracted three times with dichloromethane, the filtrate was separated, and the filtrate was adjusted to pH 2 with 10% hydrochloric acid.Crystallization, filtration, and drying to obtain pale yellow ellagic acid.Its yield was 84%.
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