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[ CAS No. 114691-92-8 ] {[proInfo.proName]}

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Chemical Structure| 114691-92-8
Chemical Structure| 114691-92-8
Structure of 114691-92-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 114691-92-8 ]

CAS No. :114691-92-8 MDL No. :MFCD00230828
Formula : C15H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :PDBQNVDCQVGALU-UHFFFAOYSA-N
M.W : 240.25 Pubchem ID :4199915
Synonyms :

Calculated chemistry of [ 114691-92-8 ]

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.07
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 69.03
TPSA : 54.37 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 3.24
Log Po/w (WLOGP) : 3.25
Log Po/w (MLOGP) : 2.71
Log Po/w (SILICOS-IT) : 3.29
Consensus Log Po/w : 2.89

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.67
Solubility : 0.0518 mg/ml ; 0.000216 mol/l
Class : Soluble
Log S (Ali) : -4.06
Solubility : 0.0212 mg/ml ; 0.0000881 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.63
Solubility : 0.00562 mg/ml ; 0.0000234 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.5

Safety of [ 114691-92-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 114691-92-8 ]

* 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 [ 114691-92-8 ]

[ 114691-92-8 ] Synthesis Path-Downstream   1~18

  • 1
  • [ 124-38-9 ]
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  • [ 114691-92-8 ]
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  • [ 108-91-8 ]
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  • 6
  • [ 114691-92-8 ]
  • [ 199678-00-7 ]
  • 2-(4-(4-(4-Acetylphenyl)benzoylamino)butyl)-7-trifluoromethylsulfonyloxy-1,2,3,4-tetrahydroisoquinoline [ No CAS ]
  • 8
  • [ 586-76-5 ]
  • [ 149104-90-5 ]
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  • 9
  • [ 619-58-9 ]
  • [ 149104-90-5 ]
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  • 10
  • [ 5731-01-1 ]
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  • 11
  • [ 114691-92-8 ]
  • N-(tert-butoxy)-4-acetyl-4'-biphenylcarboxylic acid amide [ No CAS ]
  • 12
  • [ 114691-92-8 ]
  • [ 114692-08-9 ]
  • 13
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  • [ 114691-99-5 ]
  • 14
  • [ 114691-92-8 ]
  • [ 114691-99-5 ]
  • 16
  • 1-cyclobutyl[1,4]diazepane dihydrochloride [ No CAS ]
  • [ 114691-92-8 ]
  • 1-{4'-[(4-cyclobutylhexahydro-1H-1,4-diazepin-1-yl)carbonyl]-4-biphenylyl}ethanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
With C11H16NPol; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20℃; for 16h; 1- (Cyclobutyl)-hexahydro-1 H-1, 4-diazepine dihydrochloride (D4) (0.15g) was stirred with diethylaminomethyl polystyrene (1. 0g), HOBT (0.045g) and 4'-acetyl-4- biphenylcarboxylic acid (0. 13g) in DCM (5ml). EDC (0. 16g) was then added and the reaction stirred at rt for 16h. The polymer supported base was filtered off and the filtrate was diluted with DCM (10mut) and washed with saturated sodium hydrogen carbonate (2 x 15ml). The organic layer was loaded directly onto a silica column eluting with 0-10% MeOH (containing 10% 0.880 ammonia solution)/DCM. The isolated free base product was dissolved in DCM (5ml) and treated with excess 1 N HCI/diethyl ether solution (1 ml) and stirred for 10min. The mixture was evaporated (co-evaporated with acetone 2 x 10ml), triturated with acetone, then dried at 50 C under high vacuum for 16h to yield the title compound (E2) as a pale solid (0.055g). MS electrospray (+ion) 377 (MH+). 1 H NMR 8 (DMSO-d6) : 10.57 (1H, s), 9.07 (2H, d, J=6.4Hz), 7.88 (4H, m), 7.60 (2H, d, J= 7.6Hz), 4.15 (1H, m), 3.82-3. 33 (6H, m), 3.02 (2H, m), 2.62 (3H, s), 2.41-1. 62 (8H, m)
  • 17
  • [ 99-90-1 ]
  • 4-(2-chloro-thien-3-yl)-benzoic acid [ No CAS ]
  • [ 114691-92-8 ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 40A 4'-acetyl(1,1'-biphenyl)-4-carboxylic acid The desired product was prepared by substituting 1-(4-bromophenyl)ethanone for 2-bromo-5-chlorothiophene in Example 29A. MS (APCI(-)) m/e 239 (M-H)-.
Example 40A 4'-acetyl(1,1'-biphenyl)-4-carboxylic acid The desired product was prepared by substituting 1-(4-bromophenyl)ethanone for 2-bromo-5-chlorothiophene in Example 29A. MS (APCI(-)) m/e 239 (M-H)-.
  • 18
  • [ 14047-29-1 ]
  • [ 99-91-2 ]
  • [ 114691-92-8 ]
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