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[ CAS No. 24673-56-1 ] {[proInfo.proName]}

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Chemical Structure| 24673-56-1
Chemical Structure| 24673-56-1
Structure of 24673-56-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 24673-56-1 ]

CAS No. :24673-56-1 MDL No. :MFCD00060511
Formula : C10H8O3 Boiling Point : -
Linear Structure Formula :- InChI Key :YMZTUCZCQMQFMK-UHFFFAOYSA-N
M.W : 176.17 Pubchem ID :600591
Synonyms :

Calculated chemistry of [ 24673-56-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.1
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.14
TPSA : 50.44 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.69
Log Po/w (XLOGP3) : 2.55
Log Po/w (WLOGP) : 2.44
Log Po/w (MLOGP) : 1.38
Log Po/w (SILICOS-IT) : 2.21
Consensus Log Po/w : 2.05

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.99
Solubility : 0.182 mg/ml ; 0.00104 mol/l
Class : Soluble
Log S (Ali) : -3.26
Solubility : 0.0976 mg/ml ; 0.000554 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.04
Solubility : 0.159 mg/ml ; 0.000902 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.41

Safety of [ 24673-56-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 24673-56-1 ]

* 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 [ 24673-56-1 ]

[ 24673-56-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24673-56-1 ]
  • [ 62058-03-1 ]
  • C20H23NO3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example B .6 Preparation of compound 7; 1 -Hydroxy- lH-benzotriazo Ie (0.001 mol) was added to a stirred mixture of 3-methylbenzofurancarboxylic acid [24673-56-1] (0.0009 mol) in dichloromethane (5 ml) and DMF (5 ml). The mixture was stirred for 10 minutes and iV-(ethyl- carbonimidoyl)-iV,iV-dimethyl-l,3-propanediamine, monohydrochloride [25952-53-8] (0.001 mol) was added. The resulting mixture was stirred for 1 hour before (lalpha,3alpha,4alpha,5beta,7alpha)-4-aminotricyclo[3.3.1.13'7]decan-l-ol [62058-03-1] (0.001 mol) was added. The reaction mixture was stirred at room temperature overnight and then (Polystyrylmethyl)-trimethylammonium bicarbonate (I g; Novabiochem Cat. No.: 01-64-0419) and Methylisocyanate polystyrene (I g; Novabiochem Cat. No.: 01-64-0169) were added. The resulting mixture was shaken for 1 hour and filtered. The filtrate was evaporated and the obtained residue was purified by flash column chromatography (eluent: CH2CyCH3OH 90/10). The product fractions were collected and the solvent was evaporated, yielding 0.144 g of compound 7.
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