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[ CAS No. 67127-91-7 ] {[proInfo.proName]}

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Chemical Structure| 67127-91-7
Chemical Structure| 67127-91-7
Structure of 67127-91-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 67127-91-7 ]

CAS No. :67127-91-7 MDL No. :MFCD00156981
Formula : C21H18O4 Boiling Point : -
Linear Structure Formula :- InChI Key :JCXIICUMJCMYAV-UHFFFAOYSA-N
M.W : 334.37 Pubchem ID :10664432
Synonyms :

Calculated chemistry of [ 67127-91-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 25
Num. arom. heavy atoms : 18
Fraction Csp3 : 0.1
Num. rotatable bonds : 7
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 95.36
TPSA : 55.76 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.32 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.98
Log Po/w (XLOGP3) : 4.25
Log Po/w (WLOGP) : 4.24
Log Po/w (MLOGP) : 3.66
Log Po/w (SILICOS-IT) : 4.32
Consensus Log Po/w : 3.89

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.66
Solubility : 0.00729 mg/ml ; 0.0000218 mol/l
Class : Moderately soluble
Log S (Ali) : -5.13
Solubility : 0.00247 mg/ml ; 0.00000737 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -7.07
Solubility : 0.0000287 mg/ml ; 0.0000000859 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.63

Safety of [ 67127-91-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 67127-91-7 ]

* 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.

  • Upstream synthesis route of [ 67127-91-7 ]

[ 67127-91-7 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 78283-37-1 ]
  • [ 67127-91-7 ]
YieldReaction ConditionsOperation in experiment
91% With sodium hydroxide In 1,4-dioxane; methanol; water for 14 h; Reflux A solution of 1.0 g (2.4 mmol) of ester 25 and 0.19 g (4.7 mmol) of sodium hydroxide in 15 mL of methanol, dioxane, and water (1:1:1) was stirred under reflux for 14 h, cooled to 25oC, and most of the organic solvents were removed from a rotary evaporator. The residue was diluted with water, acidified with 1 N HCl, extracted twice with ethyl acetate (50 mL), and the ethyl acetate layers were combined, washed with water and brine, dried (MgSO4), concentrated, and column chromatographed using a mixture of hexane and ethyl acetate (1:1) as eluent to give 0.72 g (91percent yield) of compound 13.15 1H NMR δ 11.06 (s, 1 H), 7.81 (d, J = 3.1 Hz, 1 H), 7.43 - 7.32 (m, 10 H), 7.17 (dd, J = 9.0, 3.1 Hz, 1 H), 7.07 (d, J = 9.0 Hz, 1 H), 5.26 (s, 2 H), 5.08 (s, 2 H); 13C NMR δ 165.3, 153.9, 151.9, 136.6, 134.6, 129.4, 129.4, 128.8, 128.4, 128.2, 127.8, 123.0, 119.0, 117.8, 115.1, 73.2, 70.9.
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 1, p. 353 - 356
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981, p. 2570 - 2576
[3] Journal of Organic Chemistry, 2004, vol. 69, # 10, p. 3530 - 3537
  • 2
  • [ 490-79-9 ]
  • [ 67127-91-7 ]
Reference: [1] Journal of Organic Chemistry, 2004, vol. 69, # 10, p. 3530 - 3537
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981, p. 2570 - 2576
  • 3
  • [ 106296-25-7 ]
  • [ 67127-91-7 ]
Reference: [1] European Journal of Medicinal Chemistry, 1997, vol. 32, # 5, p. 409 - 423
  • 4
  • [ 2150-46-1 ]
  • [ 67127-91-7 ]
Reference: [1] European Journal of Medicinal Chemistry, 1997, vol. 32, # 5, p. 409 - 423
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