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[ CAS No. 5748-41-4 ] {[proInfo.proName]}

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Chemical Structure| 5748-41-4
Chemical Structure| 5748-41-4
Structure of 5748-41-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5748-41-4 ]

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Product Details of [ 5748-41-4 ]

CAS No. :5748-41-4 MDL No. :MFCD03424592
Formula : C13H9ClO2 Boiling Point : -
Linear Structure Formula :- InChI Key :FIMRRWLTRBEAOM-UHFFFAOYSA-N
M.W : 232.66 Pubchem ID :616002
Synonyms :

Calculated chemistry of [ 5748-41-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 63.85
TPSA : 37.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.15
Log Po/w (XLOGP3) : 4.38
Log Po/w (WLOGP) : 3.71
Log Po/w (MLOGP) : 3.68
Log Po/w (SILICOS-IT) : 3.53
Consensus Log Po/w : 3.49

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.46
Solubility : 0.00798 mg/ml ; 0.0000343 mol/l
Class : Moderately soluble
Log S (Ali) : -4.88
Solubility : 0.00307 mg/ml ; 0.0000132 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.91
Solubility : 0.00286 mg/ml ; 0.0000123 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.59

Safety of [ 5748-41-4 ]

Signal Word:Danger Class:9
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P330-P362+P364-P403+P233-P501 UN#:3077
Hazard Statements:H302-H315-H318-H335-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5748-41-4 ]

* 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 [ 5748-41-4 ]

[ 5748-41-4 ] Synthesis Path-Downstream   1~2

  • 2
  • aq. sodium bisulfite [ No CAS ]
  • [ 80565-30-6 ]
  • [ 5748-41-4 ]
YieldReaction ConditionsOperation in experiment
With oxone; ethylenediaminetetraacetic acid; sodium hydrogencarbonate; In levulinonitrile; water; toluene; 4-(4-Chlorophenyl)benzoic Acid To a stirred solution of 4-(4-chlorophenyl)benzaldehyde (0.84 g, 3.9 mmol) in 30 mL acetonitrile-acetone (2: 1) is added 15 mL water and solid sodium bicarbonate (3.5 g, 41.7 mmol). After 5 min. a 25 mL solution of oxidation reagent (Oxone: 4.8 g, 7.8 mmol in 25 mL water containing 4*10-4 M EDTA) is added dropwise over 15 min. then stirred for an additional 3.5 h. The reaction mixture is then treated with 18 mL aq. sodium bisulfite (9.5 g), stirred 2 h, then acidified with 10 mL 6 M HCl. The mixture is transferred to a separatory funnel and diluted with 300 mL dichloromethane and 400 mL water. The water layer is washed with dichloromethane (3*120 mL), organic layers combined, then washed with 500 mL water. The organic layer is dried over sodium sulfate, filtered, and evaporated under reduced pressure. The desired acid is crystallized from acetone-water (5:2), filtered, washed with water, and evaporated under reduced pressure from toluene affording 0.6 g product. Remaining product could be isolated by chromatography but the amount obtained is satisfactory. TLC: Rf=0.3 (chloroform-methanol; 10:1).
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