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[ CAS No. 497-18-7 ] {[proInfo.proName]}

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Chemical Structure| 497-18-7
Chemical Structure| 497-18-7
Structure of 497-18-7 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 497-18-7 ]

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Product Details of [ 497-18-7 ]

CAS No. :497-18-7 MDL No. :MFCD00007591
Formula : CH6N4O Boiling Point : -
Linear Structure Formula :- InChI Key :XEVRDFDBXJMZFG-UHFFFAOYSA-N
M.W : 90.08 Pubchem ID :73948
Synonyms :

Calculated chemistry of [ 497-18-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 6
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 4.0
Molar Refractivity : 18.53
TPSA : 93.17 ?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 : No
Log Kp (skin permeation) : -7.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : -0.08
Log Po/w (XLOGP3) : -1.57
Log Po/w (WLOGP) : -1.97
Log Po/w (MLOGP) : -1.66
Log Po/w (SILICOS-IT) : -1.37
Consensus Log Po/w : -1.33

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.72
Solubility : 476.0 mg/ml ; 5.28 mol/l
Class : Highly soluble
Log S (Ali) : 0.12
Solubility : 119.0 mg/ml ; 1.32 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.88
Solubility : 688.0 mg/ml ; 7.64 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.63

Safety of [ 497-18-7 ]

Signal Word:Danger Class:9
Precautionary Statements:P501-P273-P260-P270-P264-P280-P391-P314-P337+P313-P305+P351+P338-P301+P312+P330 UN#:3077
Hazard Statements:H302-H319-H372-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 497-18-7 ]

* 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 [ 497-18-7 ]

[ 497-18-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 497-18-7 ]
  • [ 40138-17-8 ]
  • [ 7732-18-5 ]
  • C17H14B2N4O2*0.25H2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
94% With formic acid; for 2h;Reflux; General procedure: To a stirred H2O (25 mL) suspension of the appropriateboronic acid-containing aldehyde (2.22 mmol) and 1 dropof formic acid was added an aqueous solution (5 mL) ofcarbohydrazide (100 mg, 1.11 mmol). Compound 7 wassynthesized using MeOH as the solvent. The reactionmixture was heated at reflux for 2 h, at which pointthe reaction was allowed to cool to room temperature(RT). The resulting precipitate was collected by suctionfiltration and washed with Et2O (2 × 10 mL) to afford thepentacyclic oxadiazadiborinanes as white or off-whitesolids.
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