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[ CAS No. 4543-47-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
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Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 4543-47-9
Chemical Structure| 4543-47-9
Structure of 4543-47-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4543-47-9 ]

CAS No. :4543-47-9 MDL No. :MFCD02681983
Formula : C5H7NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :XNABHFLZYMCJHE-UHFFFAOYSA-N
M.W : 97.12 Pubchem ID :2776197
Synonyms :

Calculated chemistry of [ 4543-47-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 26.38
TPSA : 39.16 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.86 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.42
Log Po/w (XLOGP3) : 0.04
Log Po/w (WLOGP) : 0.59
Log Po/w (MLOGP) : -0.47
Log Po/w (SILICOS-IT) : 0.94
Consensus Log Po/w : 0.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.93
Solubility : 11.4 mg/ml ; 0.118 mol/l
Class : Very soluble
Log S (Ali) : -0.42
Solubility : 37.3 mg/ml ; 0.385 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.57
Solubility : 2.6 mg/ml ; 0.0268 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 4543-47-9 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P280-P301+P310+P330-P305+P351+P338-P337+P313-P405-P501 UN#:2810
Hazard Statements:H301-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 4543-47-9 ]

* 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 [ 4543-47-9 ]

[ 4543-47-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4543-47-9 ]
  • [ 53554-29-3 ]
  • ethyl 2-((furan-2-ylmethyl)amino)-4-hydroxypyrimidine-5-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
63.3% In ethanol; for 24h;Reflux; Sealed tube; General procedure: To a Radley reaction carousel tube, add 1 equivalent 1, 1.1 equivalents of the amine, a stir bar, and 5 mL 95% ethanol. Reflux while stirring for 24 hours. After cooling to room temperature the resulting precipitate was collected by vacuum filtration, washing with 10 mL deionized water and 5 mL chloroform.
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