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[ CAS No. 941-98-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 941-98-0
Chemical Structure| 941-98-0
Structure of 941-98-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 941-98-0 ]

CAS No. :941-98-0 MDL No. :MFCD00004013
Formula : C12H10O Boiling Point : -
Linear Structure Formula :(C10H7)C(O)CH3 InChI Key :QQLIGMASAVJVON-UHFFFAOYSA-N
M.W : 170.21 Pubchem ID :13663
Synonyms :
Chemical Name :1'-Acetonaphthone

Calculated chemistry of [ 941-98-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.08
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 54.14
TPSA : 17.07 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.05
Log Po/w (XLOGP3) : 2.86
Log Po/w (WLOGP) : 3.04
Log Po/w (MLOGP) : 2.76
Log Po/w (SILICOS-IT) : 3.33
Consensus Log Po/w : 2.81

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.2
Solubility : 0.107 mg/ml ; 0.00063 mol/l
Class : Soluble
Log S (Ali) : -2.88
Solubility : 0.226 mg/ml ; 0.00133 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.4
Solubility : 0.00673 mg/ml ; 0.0000395 mol/l
Class : Moderately soluble

Medicinal Chemistry

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

Safety of [ 941-98-0 ]

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

Application In Synthesis of [ 941-98-0 ]

* 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 [ 941-98-0 ]

[ 941-98-0 ] Synthesis Path-Downstream   1~10

  • 2
  • [ 941-98-0 ]
  • [ 50-00-0 ]
  • [ 80567-00-6 ]
  • 3-(2,6-dimethyl-morpholin-4-yl)-1-naphthalen-1-yl-propan-1-one [ No CAS ]
  • 3
  • [ 941-98-0 ]
  • [ 51012-64-7 ]
  • [ 1014981-18-0 ]
  • 4
  • [ 941-98-0 ]
  • [ 16732-66-4 ]
  • [ 1176887-37-8 ]
  • 5
  • [ 941-98-0 ]
  • [ 6914-71-2 ]
  • C18H16O4 [ No CAS ]
  • 6
  • [ 941-98-0 ]
  • [ 110677-45-7 ]
  • [ 1367364-45-1 ]
YieldReaction ConditionsOperation in experiment
68% With sodium hydroxide; In ethanol; chloroform; at 20℃; The 816 mg (4.8mmol) α- acetonaphthone , 240 mg (6mmol) sodium hydroxide in 100 ml of water, adding 6 ml ethanol, 12 drip enable its dissolution. The 1302 mg (4.8mmol) 4-(9-(9H-carbazolyl)) benzaldehyde dissolved in 18 ml in chloroform, in the above-mentioned is dripped into the ethanol solution, stirring the mixture at room temperature for overnight, to stop the reaction. Overhanging organic solvent, water and dilute, dichloromethane extraction, drying, recrystallized (petroleum ether: ethyl acetate = 15 the [...] 1), to get the yellow cluster crystal a1.37g, yield = 68%.
  • 7
  • [ 941-98-0 ]
  • [ 6374-91-0 ]
  • [ 6913-87-7 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In ethanol; water; at 20℃; for 2h; General procedure: An aqueous solution of sodium hydroxide (5%, 10mL) was added slowly to the stirring solution of isatin (1mmol) and appropriate aryl acetophenone (1mmol) in ethanol (20mL) in 100mL conical flask. The stirring was continued for 2h and the completion of reaction was monitored by TLC. The reaction on completion was poured onto ice, solid obtained after filtration was crystallized from ethanol. The physical data for the characteristic compound is shown below:
  • 8
  • [ 941-98-0 ]
  • [ 5572-94-1 ]
  • 1-(2-(4-iodophenyl)naphthalene-1-yl)ethan-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With tris(triphenylphosphine)ruthenium(II) chloride; caesium carbonate; at 150℃; for 3h;Inert atmosphere; Under an argon atmosphere, carbonylchloro hydride tris (triphenylphosphine)ruthenium 4.8 mg (5.0μmol), 2-(4- iodophenyl) -5,5 - dimethyl -1, 3, 2 - dioxaborinane 316 mg (1.00mmol), cesium carbonate 97.8mg (300μmol) and 1 - acetonaphthone 1.12 mg (6.58 mmol) are added in a reactioncontainer. The reactionvessel is heated on 135 ,and it is stirred for 12 hour. After thereaction vessel cooled as room temperature,mixture is purified by using silica gel columnchromatography (hexane : ethyl acetate = 10 : 0-9 : 1), 260 mg of 1 - [2 - (4- iodophenyl) naphthalene - 1- yl] ethanone obtained (white solid, yield 70%).
  • 9
  • [ 766-36-9 ]
  • [ 941-98-0 ]
  • (E)-3-ethyl-4-methyl-5-(1-(naphthalen-3-yl)ethylidene)-1H-pyrrol-2(5H)-one [ No CAS ]
  • 10
  • [ 766-36-9 ]
  • [ 941-98-0 ]
  • (Z)-3-ethyl-4-methyl-5-(1-(naphthalen-3-yl)ethylidene)-1H-pyrrol-2(5H)-one [ No CAS ]
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