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[ CAS No. 74073-22-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 74073-22-6
Chemical Structure| 74073-22-6
Structure of 74073-22-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 74073-22-6 ]

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Product Details of [ 74073-22-6 ]

CAS No. :74073-22-6 MDL No. :MFCD00800930
Formula : C12H10Cl2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :QQXPSPWWWCQBFM-RMKNXTFCSA-N
M.W : 273.11 Pubchem ID :11821770
Synonyms :

Calculated chemistry of [ 74073-22-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 67.27
TPSA : 43.37 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.76 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.54
Log Po/w (XLOGP3) : 3.1
Log Po/w (WLOGP) : 3.03
Log Po/w (MLOGP) : 2.88
Log Po/w (SILICOS-IT) : 3.67
Consensus Log Po/w : 3.05

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.48
Solubility : 0.0897 mg/ml ; 0.000328 mol/l
Class : Soluble
Log S (Ali) : -3.68
Solubility : 0.0572 mg/ml ; 0.000209 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.13
Solubility : 0.0202 mg/ml ; 0.000074 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.6

Safety of [ 74073-22-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 74073-22-6 ]

* 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 [ 74073-22-6 ]

[ 74073-22-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 74073-22-6 ]
  • [ 626-34-6 ]
  • [ 72509-76-3 ]
YieldReaction ConditionsOperation in experiment
at 90℃; for 0.15h;Microwave irradiation; General procedure: A mixture of the aldehyde 1 (2 mmol), the 1,3-dicarbonyl compound 2 (2 mmol) and the 3D printed Al2O3 structure (0.350 g) was submitted to microwave irradiation (120 C) for in coated vial. Once the aldehyde component was consumed (TLC control) the corresponding 3-aminocrotonate 6 (2 mmol) was added and the mixture heated at 90 C (microwave irradiation). After completion of the reaction, as indicated by TLC, the mixture was cooled and the desired compound solidified. For those 1,4-dihydropyridines that not solidified, the reaction mixture was poured onto crushed ice and stirred for 5-10 min. The solid obtained was filtered under suction, washed with ice-cold water (20 mL) and then purified by column chromatography or recrystallization from the appropriate solvent.
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Technical Information

? Acyl Group Substitution ? Alkyl Halide Occurrence ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Bouveault-Blanc Reduction ? Bucherer-Bergs Reaction ? Catalytic Hydrogenation ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Ester Cleavage ? Fischer Indole Synthesis ? General Reactivity ? Grignard Reaction ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? 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 ? Reactions with Organometallic Reagents ? Reformatsky Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Tebbe Olefination ? Ugi Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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