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[ CAS No. 2450-26-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2450-26-2
Chemical Structure| 2450-26-2
Structure of 2450-26-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2450-26-2 ]

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Product Details of [ 2450-26-2 ]

CAS No. :2450-26-2 MDL No. :MFCD00017020
Formula : C8H7NO5 Boiling Point : -
Linear Structure Formula :- InChI Key :PHCNQUJHXJQLQR-UHFFFAOYSA-N
M.W : 197.14 Pubchem ID :96959
Synonyms :

Calculated chemistry of [ 2450-26-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.17
TPSA : 92.35 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.89
Log Po/w (XLOGP3) : 0.83
Log Po/w (WLOGP) : 1.12
Log Po/w (MLOGP) : -0.52
Log Po/w (SILICOS-IT) : -0.62
Consensus Log Po/w : 0.34

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.7
Solubility : 3.89 mg/ml ; 0.0198 mol/l
Class : Very soluble
Log S (Ali) : -2.35
Solubility : 0.877 mg/ml ; 0.00445 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.28
Solubility : 10.3 mg/ml ; 0.052 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.07

Safety of [ 2450-26-2 ]

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

Application In Synthesis of [ 2450-26-2 ]

* 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 [ 2450-26-2 ]

[ 2450-26-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 2450-26-2 ]
  • [ 57616-74-7 ]
  • 3-methoxy-4-[3-(morpholin-4-yl)propoxy]-2-nitrobenzaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
854 g of <strong>[57616-74-7]4-<strong>[57616-74-7](3-chloropropyl)morpholine hydrochloride</strong></strong> were suspended in 19.4 L of acetonitrile and the mixture was stirred for 50 min. at r.t.. The mixture was filtered, and the residue was washed with 0.7 L of acetonitrile. The filtrate was dosed to a suspension of 700 g of 2-nitrovanilline and 1 .96 kg of potassium carbonate in 7 L of acetonitrile at r.t. over a period of ca. 2 h. The reaction mixture was heated to reflux, and stirred at reflux for 3 h. The mixture was cooled to r.t., and filtered. The residue was washed twice with acetonitrile. The filtrate was concentrated under vacuum and the residue dissolved in 5.6 L of ethyl acetate. This solution is washed with 7 L of aqueous 10 w% sodium chloride solution, then 7.7 L of aqueous 1 % sodium chloride solution. After removal of the solvent, the viscous residue of ca. 1 .14 kg was dissolved in 2.3 L of dichloromethane, the solvent of the next step. 1 H-NMR (500 MHz, de-DMSO): d = 1 .97 (m, 2H); 2.36 (m, 4 H); 2.45 (t, 2H); 3.56 (m, 4H); 3.85 (s, 3H); 4.27 (t, 2H); 7.51 (d, 1 H); 7.87 (d, 1 H); 9.80 (s, 1 H).
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Technical Information

? Acidity of Phenols ? Alkyl Halide Occurrence ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nomenclature of Ethers ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Ethers ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Ethers ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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