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[ CAS No. 38148-63-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 38148-63-9
Chemical Structure| 38148-63-9
Structure of 38148-63-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 38148-63-9 ]

CAS No. :38148-63-9 MDL No. :MFCD00136405
Formula : C7H9ClN2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :VHVJRSVTZPYXEH-UHFFFAOYSA-N
M.W : 172.61 Pubchem ID :217124
Synonyms :

Calculated chemistry of [ 38148-63-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 3.0
Molar Refractivity : 46.69
TPSA : 70.1 ?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) : -6.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.64
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 1.32
Log Po/w (SILICOS-IT) : 0.63
Consensus Log Po/w : 0.81

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.65
Solubility : 3.86 mg/ml ; 0.0223 mol/l
Class : Very soluble
Log S (Ali) : -1.69
Solubility : 3.55 mg/ml ; 0.0205 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.52
Solubility : 5.15 mg/ml ; 0.0299 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 38148-63-9 ]

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

Application In Synthesis of [ 38148-63-9 ]

* 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 [ 38148-63-9 ]

[ 38148-63-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52133-67-2 ]
  • [ 38148-63-9 ]
  • [ 1199942-97-6 ]
YieldReaction ConditionsOperation in experiment
4-Hydroxybenzamidine hydrochloride (15.2 g) was dissolved in absolute ethanol (520 ml.) and a part of the ethanol (370 ml.) was subsequently distilled off again. More absolute ethanol (370 ml.) was added to this receiving solution, together with DBU (30 ml_), <strong>[52133-67-2]2-cyano-4,4-diethoxy-butyric acid ethyl ester</strong> (40.0 g) and triethyl amine (26 ml_). The resulting mixture was heated until reflux and further refluxed for 45 hours ("hrs"). Most of the solvent (430 ml.) was then distilled off while the remainder was allowed to cool to 50 0C. An aqueous solution of hydrochloric acid (2.3 M, 229 ml.) was added dropwise, then the reaction mixture was allowed to cool to ambient temperature and stirring was continued for 1 hr. The resulting precipitate was filtered off, washed with water (3 x 100 ml.) and dried in vacuo at 40 0C to yield 16.0 g 2-(4-hydroxy-phenyl)-7/-/-pyrrolo[2,3-d]pyrimidin-4-ol
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