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[ CAS No. 104-93-8 ] {[proInfo.proName]}

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Chemical Structure| 104-93-8
Chemical Structure| 104-93-8
Structure of 104-93-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 104-93-8 ]

CAS No. :104-93-8 MDL No. :MFCD00008413
Formula : C8H10O Boiling Point : -
Linear Structure Formula :- InChI Key :CHLICZRVGGXEOD-UHFFFAOYSA-N
M.W : 122.16 Pubchem ID :7731
Synonyms :
4-Methoxytoluene
Chemical Name :1-Methoxy-4-methylbenzene

Calculated chemistry of [ 104-93-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.9
TPSA : 9.23 ?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) : -5.16 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.14
Log Po/w (XLOGP3) : 2.66
Log Po/w (WLOGP) : 2.0
Log Po/w (MLOGP) : 2.14
Log Po/w (SILICOS-IT) : 2.31
Consensus Log Po/w : 2.25

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.7
Solubility : 0.243 mg/ml ; 0.00199 mol/l
Class : Soluble
Log S (Ali) : -2.51
Solubility : 0.382 mg/ml ; 0.00312 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.87
Solubility : 0.167 mg/ml ; 0.00136 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 104-93-8 ]

Signal Word:Danger Class:3
Precautionary Statements:P273-P280 UN#:1993
Hazard Statements:H225-H302-H315-H361-H412 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 104-93-8 ]

* 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 [ 104-93-8 ]

[ 104-93-8 ] Synthesis Path-Downstream   1~15

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YieldReaction ConditionsOperation in experiment
69% With aluminum (III) chloride; In dichloromethane; at 0 - 20℃; for 3h; l-(2-Metho l)-ethanoneI -(2-M elhoxy-5-methy]-pheny])-ethanoncLambda solution of acetyl chloride (6.79 ml, 95.1 mmol). l-Methoxy-4-methyl-benzene (intermediate LXXXVII) (9.69 g, 79.4 mmol) in 50 ml of dichloromethane was added dropwise to a suspension of aluminium chloride (12.69 g, 95.1 mmol) in 50 ml of dichloromethane at 0 C. rPhen the reaction mixture was stirred at room temperature for 3 hours. Then the reaction mixture was quenched with 1.5 N hydrochloric acid solution and extracted with dichloromethane. The combined organic extract was washed with water. brine, dried over anhydrous sodium sulphate and evaporated. The crude material was purified using column chromatography (silica gel 100-200 mesh, 15:85 ethylacetate:hexane) to afford l-(2-Methoxy-5-methyl-phenyl)-ethanone in 69 % yield. ?-Iota NMR (400 MHz, CDCI3): 7.528 (s, JH), 7.247 (bs, lH), 6.852-6.873 (d, 111, J=8.4 Hz), 3.881 (s, 3H), 2.601 (s, 3H), 2.299 (s, 3H).
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