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[ CAS No. 5527-95-7 ] {[proInfo.proName]}

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Chemical Structure| 5527-95-7
Chemical Structure| 5527-95-7
Structure of 5527-95-7 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5527-95-7 ]

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Product Citations

Product Details of [ 5527-95-7 ]

CAS No. :5527-95-7 MDL No. :MFCD00143288
Formula : C7H4ClFO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 158.56 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 5527-95-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.8
TPSA : 17.07 ?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) : -5.77 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 2.11
Log Po/w (WLOGP) : 2.71
Log Po/w (MLOGP) : 2.48
Log Po/w (SILICOS-IT) : 3.04
Consensus Log Po/w : 2.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.53
Solubility : 0.468 mg/ml ; 0.00295 mol/l
Class : Soluble
Log S (Ali) : -2.1
Solubility : 1.26 mg/ml ; 0.00796 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.23
Solubility : 0.0938 mg/ml ; 0.000592 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.16

Safety of [ 5527-95-7 ]

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 [ 5527-95-7 ]

* 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 [ 5527-95-7 ]

[ 5527-95-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 2612-28-4 ]
  • [ 5527-95-7 ]
  • [ 136466-71-2 ]
YieldReaction ConditionsOperation in experiment
toluene-4-sulfonic acid; In toluene; for 2h;Heating / reflux; 3.2 g (20 mmol) of the aldehyde 18 and 4.7 g (30 mmol) of the 1,3-diol are dissolved in 50 ml of toluene, 0.4 g of p-toluenesulfonic acid is added, and the mixture is heated on a water separator for 2 h. The cooled solution is washed with sat. sodium hydrogencarbonate solution and evaporated. The residue is passed through silica gel.
  • 2
  • [ 13781-53-8 ]
  • [ 5527-95-7 ]
  • [ 1619942-59-4 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; In methanol; at 20℃; General procedure: In the first synthetic step (step a, Scheme 1), a series of (Z)-substituted diarylacrylonitrile analogues were synthesized by reacting substituted benzyl carbaldehydes with their corresponding substituted phenylacetonitriles in 5% NaOMe in methanol. The reaction mixture was stirred at room temperature for 2-3 h for the reaction to complete and the final product precipitated of the solution. The precipitate was filtered, washed with water and dried to yield the final compound in yields ranging from 70 to 95% (Scheme 1) [16].
  • 3
  • [ 2612-28-4 ]
  • [ 5527-95-7 ]
  • 2-(4-chloro-3-fluorophenyl)-5-propyl-1,3-dioxane [ No CAS ]
YieldReaction ConditionsOperation in experiment
30.9g With toluene-4-sulfonic acid; In toluene;Inert atmosphere; Reflux; Dean-Stark; Under a nitrogen atmosphere, 4-chloro-3-fluorobenzaldehyde (25 g), <strong>[2612-28-4]2-propyl-1,3-propanediol</strong> (18.6 g), and p- toluenesulfonic acid monohydrate (0 the .90g) was dissolved in toluene (500mL), it was brought to reflux.The resulting water was removed using a Dean-Stark apparatus, and stirred for further 30 minutes.Was allowed to cool to room temperature, the addition of a saturated aqueous solution of sodium hydrogen carbonate (200mL) were separated, and the organic layer was washed with saturated brine (200mL), and dried over anhydrous sodium sulfate, evaporated under reduced pressure and the organic solvent did.The residue was purified by silica gel column chromatography, and recrystallized from methanol to give 2- (4-chloro-3-fluoro-phenyl) -5-propyl-1,3-dioxane (30.9g).
  • 4
  • [ 2612-28-4 ]
  • [ 5527-95-7 ]
  • trans-2-[4-(4-(difluoro(5,6,7-trifluoronaphthalen-2-oxy)methyl)-3,5-difluorophenyl)-3-fluorophenyl]-5-propyl-1,3-dioxane [ No CAS ]
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Technical Information

? Alkyl Halide Occurrence ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Kinetics of Alkyl Halides ? Knoevenagel Condensation ? Kumada Cross-Coupling Reaction ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nozaki-Hiyama-Kishi Reaction ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
Historical Records

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