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[ CAS No. 65874-27-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 65874-27-3
Chemical Structure| 65874-27-3
Structure of 65874-27-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 65874-27-3 ]

Related Doc. of [ 65874-27-3 ]

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Product Citations

Product Details of [ 65874-27-3 ]

CAS No. :65874-27-3 MDL No. :MFCD01111994
Formula : C12H14O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :DUNFNBQQWYQKFE-UHFFFAOYSA-N
M.W : 206.24 Pubchem ID :2751588
Synonyms :

Calculated chemistry of [ 65874-27-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 57.57
TPSA : 43.37 ?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) : -5.98 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.35
Log Po/w (XLOGP3) : 2.22
Log Po/w (WLOGP) : 2.45
Log Po/w (MLOGP) : 2.16
Log Po/w (SILICOS-IT) : 2.64
Consensus Log Po/w : 2.37

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.55
Solubility : 0.582 mg/ml ; 0.00282 mol/l
Class : Soluble
Log S (Ali) : -2.77
Solubility : 0.354 mg/ml ; 0.00172 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.25
Solubility : 0.116 mg/ml ; 0.000561 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.47

Safety of [ 65874-27-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 65874-27-3 ]

* 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 [ 65874-27-3 ]

[ 65874-27-3 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 65874-27-3 ]
  • [ 1134776-39-8 ]
  • 3
  • [ 65874-27-3 ]
  • [ 105580-41-4 ]
  • 4
  • [ 65874-27-3 ]
  • [ 1791-13-5 ]
  • (S)-di-tert-butyl 2-((4-(tert-butoxycarbonyl)benzyl)amino)succinate [ No CAS ]
YieldReaction ConditionsOperation in experiment
346.1 mg A) (S)-Di-tert-butyl 2-((4-(tert-butoxycarbonyl)benzyl)amino) succinate Acetic acid (0.212 mL) was added to a mixture of <strong>[1791-13-5]L-<strong>[1791-13-5]aspartic acid di-tert-butyl ester hydrochloride</strong></strong> (418 mg), tert-butyl 4-formylbenzoate (306 mg), and THF (8 mL) at room temperature, followed by stirring at the same temperature for 1 hour. Sodium triacetoxyborohydride (786 mg) was added to the reaction mixture at room temperature, followed by stirring at the same temperature overnight. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture at 0 C., followed by extraction with ethyl acetate. The organic layer was washed with a saturated saline solution and was then dried over anhydrous magnesium sulfate, and the solvent was distilled under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (346.1 mg). MS: [M+H]+ 436.2.
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Technical Information

? Acyl Group Substitution ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bouveault-Blanc Reduction ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Catalytic Hydrogenation ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Ester Cleavage ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation ? Hantzsch Dihydropyridine Synthesis ? Heat of Combustion ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? Mannich 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 Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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