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[ CAS No. 708-76-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 708-76-9
Chemical Structure| 708-76-9
Structure of 708-76-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 708-76-9 ]

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Product Details of [ 708-76-9 ]

CAS No. :708-76-9 MDL No. :MFCD00003328
Formula : C9H10O4 Boiling Point : -
Linear Structure Formula :- InChI Key :FQRQWPNYJOFDLO-UHFFFAOYSA-N
M.W : 182.17 Pubchem ID :69725
Synonyms :

Calculated chemistry of [ 708-76-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.84
TPSA : 55.76 ?2

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) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.17
Log Po/w (XLOGP3) : 1.52
Log Po/w (WLOGP) : 1.22
Log Po/w (MLOGP) : 0.24
Log Po/w (SILICOS-IT) : 1.51
Consensus Log Po/w : 1.33

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.07
Solubility : 1.55 mg/ml ; 0.0085 mol/l
Class : Soluble
Log S (Ali) : -2.3
Solubility : 0.914 mg/ml ; 0.00502 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.03
Solubility : 1.72 mg/ml ; 0.00942 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.38

Safety of [ 708-76-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 708-76-9 ]

* 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 [ 708-76-9 ]

[ 708-76-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 708-76-9 ]
  • [ 326-62-5 ]
  • 5,7-dimethoxy-3-(2'-fluorophenyl)iminocoumarin [ No CAS ]
  • 2
  • [ 6964-21-2 ]
  • [ 708-76-9 ]
  • C15H14O5S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With dicyclohexyl-carbodiimide; In dimethyl sulfoxide; at 110℃; General procedure: A solution of ortho-hydroxybenzaldehyde (1-4, 8 mmol), substituted acetic acid (a-c, 10 mmol) and DCC (12 mmol) in dimethylsulfoxide (DMSO, 10 mL), was heated (oil bath) at 110 C for 24-48 h. On completion of the reaction, cold water (100 mL) and acetic acid (15 mL) were added. The reaction mixture was stirred at room temperature for 4 h and extracted with diethyl ether (4 × 100 mL). The precipitated dicyclohexylurea was filtered off. The filtrate was extracted with 5% aqueous NaHCO3 (200 mL). The organic phase was stirred for 1 h with 5% aqueous sodium metabisulfite in order to remove the unreacted hydroxybenzaldehyde. The organic phase was washed with water, dried (Na2SO4) and the solvent removed under reduced pressure. The residue was purified by column chromatography (Hexane/EtOAc, 9:1).
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Technical Information

? Acidity of Phenols ? 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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