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[ CAS No. 23088-52-0 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 23088-52-0
Chemical Structure| 23088-52-0
Chemical Structure| 23088-52-0
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Product Details of [ 23088-52-0 ]

CAS No. :23088-52-0 MDL No. :MFCD00464227
Formula : C10H8N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :ASVXNFGUPSDDTA-UHFFFAOYSA-N
M.W : 188.18 Pubchem ID :541773
Synonyms :

Calculated chemistry of [ 23088-52-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.03
TPSA : 69.12 Ų

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) : -6.18 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.84
Log Po/w (XLOGP3) : 1.78
Log Po/w (WLOGP) : 1.44
Log Po/w (MLOGP) : 0.63
Log Po/w (SILICOS-IT) : 1.55
Consensus Log Po/w : 1.45

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.58
Solubility : 0.498 mg/ml ; 0.00265 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.266 mg/ml ; 0.00141 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.35
Solubility : 0.0846 mg/ml ; 0.00045 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.57

Safety of [ 23088-52-0 ]

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

Application In Synthesis of [ 23088-52-0 ]

* 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.

  • Upstream synthesis route of [ 23088-52-0 ]
  • Downstream synthetic route of [ 23088-52-0 ]

[ 23088-52-0 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 51677-09-9 ]
  • [ 23088-52-0 ]
Reference: [1] Journal of Heterocyclic Chemistry, 2003, vol. 40, # 6, p. 1097 - 1102
  • 2
  • [ 51677-09-9 ]
  • [ 7664-41-7 ]
  • [ 23088-52-0 ]
Reference: [1] Indian Journal of Heterocyclic Chemistry, 2011, vol. 20, # 3, p. 279 - 280
  • 3
  • [ 20577-73-5 ]
  • [ 23088-52-0 ]
Reference: [1] Journal of Heterocyclic Chemistry, 2003, vol. 40, # 6, p. 1097 - 1102
  • 4
  • [ 17557-81-2 ]
  • [ 536-74-3 ]
  • [ 23088-52-0 ]
Reference: [1] Tetrahedron, 1985, vol. 41, # 4, p. 727 - 738
  • 5
  • [ 14441-90-8 ]
  • [ 23088-52-0 ]
Reference: [1] Gazzetta Chimica Italiana, 1942, vol. 72, p. 155,162, 458, 466
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Technical Information

• 1,4-Addition of an Amine to a Conjugated Enone • 1,4-Addition of an Amine to a Conjugated Enone • Acyl Group Substitution • Amide Hydrolysis • Amide Hydrolysis • Amides Can Be Converted into Aldehydes • Amine Synthesis from Nitriles • Amine Synthesis from Nitriles • Amines Convert Acyl Chlorides into Amides • Amines Convert Esters into Amides • Azide Reduction by LiAlH4 • Azide Reduction by LiAlH4 • Basicity of Amines • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Chichibabin Reaction • Complex Metal Hydride Reductions • Diazotization Reaction • DIBAL Attack Nitriles to Give Ketones • Enamine Formation • Formation of an Amide from an Amine and a Carboxylic Acid • Formation of an Amide from an Amine and a Carboxylic Acid • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hofmann Elimination • Hofmann Rearrangement • Hydride Reductions • Hydrolysis of Imines to Aldehydes and Ketones • Imine Formation from Amines and Aldehydes or Ketones • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitrosation of Amines • Peptide Bond Formation with DCC • Petasis Reaction • Preparation of Amines • Preparation of LDA • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reduction of an Amide to an Amine • Reduction of an Amide to an Amine • Reductive Amination • Reductive Amination • Ring Opening of Azacyclopropanes • Ring Opening of Azacyclopropanes • Ring Opening of Oxacyclobutanes • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Strecker Synthesis • Synthesis of 2-Amino Nitriles • Ugi Reaction
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