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[ CAS No. 1504-74-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1504-74-1
Chemical Structure| 1504-74-1
Structure of 1504-74-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1504-74-1 ]

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Product Details of [ 1504-74-1 ]

CAS No. :1504-74-1 MDL No. :MFCD00007001
Formula : C10H10O2 Boiling Point : -
Linear Structure Formula :C6H6COC2H2OCH2 InChI Key :KKVZAVRSVHUSPL-GQCTYLIASA-N
M.W : 162.19 Pubchem ID :641298
Synonyms :
o-Methoxycinnamaldehyde

Calculated chemistry of [ 1504-74-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.1
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 48.03
TPSA : 26.3 ?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) : -5.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.01
Log Po/w (XLOGP3) : 2.2
Log Po/w (WLOGP) : 1.8
Log Po/w (MLOGP) : 1.66
Log Po/w (SILICOS-IT) : 2.48
Consensus Log Po/w : 2.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.4
Solubility : 0.64 mg/ml ; 0.00395 mol/l
Class : Soluble
Log S (Ali) : -2.39
Solubility : 0.666 mg/ml ; 0.00411 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.55
Solubility : 0.454 mg/ml ; 0.0028 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.87

Safety of [ 1504-74-1 ]

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

Application In Synthesis of [ 1504-74-1 ]

* 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 [ 1504-74-1 ]

[ 1504-74-1 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 2478-38-8 ]
  • [ 1504-74-1 ]
  • [ 1356939-69-9 ]
YieldReaction ConditionsOperation in experiment
28% General procedure: A solution of the 2.5 mmol of the appropriate acetophenone, indanone, tetralone derivative or 1,3-diacteylbenzene and 2mL 50% NaOH in 10mL ethanol was stirred at room temperature for 30min. Then, 2.5mmol (or 5mmol with 1,3-diacetylbenzene) of the corresponding benzaldehyde or cinnamaldehyde derivative, dissolved in 1mL ethanol, were added and stirred at room temperature After conversion of the starting compounds was completed as monitored by TLC, the reaction mixture was poured into ice water and acidified with 10% HCl to pH 6. The so-formed solid was filtered off and the crude product was further purified by recrystallization in ethanol.
  • 3
  • [ 1504-74-1 ]
  • [ 176957-55-4 ]
  • C25H22O3S2 [ No CAS ]
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