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[ CAS No. 23996-25-0 ] {[proInfo.proName]}

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Chemical Structure| 23996-25-0
Chemical Structure| 23996-25-0
Structure of 23996-25-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 23996-25-0 ]

CAS No. :23996-25-0 MDL No. :MFCD00051492
Formula : C9H13N3 Boiling Point : -
Linear Structure Formula :- InChI Key :UIDDPPKZYZTEGS-UHFFFAOYSA-N
M.W : 163.22 Pubchem ID :90327
Synonyms :

Calculated chemistry of [ 23996-25-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.56
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.59
TPSA : 41.61 ?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) : -6.68 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.68
Log Po/w (XLOGP3) : 0.87
Log Po/w (WLOGP) : 1.67
Log Po/w (MLOGP) : 0.35
Log Po/w (SILICOS-IT) : 1.72
Consensus Log Po/w : 1.26

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.51
Solubility : 5.04 mg/ml ; 0.0309 mol/l
Class : Very soluble
Log S (Ali) : -1.33
Solubility : 7.67 mg/ml ; 0.047 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.48
Solubility : 0.547 mg/ml ; 0.00335 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.14

Safety of [ 23996-25-0 ]

Signal Word:Danger Class:8,6.1
Precautionary Statements:P261-P280-P301+P310-P305+P351+P338 UN#:2922
Hazard Statements:H301-H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 23996-25-0 ]

* 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.

  • Downstream synthetic route of [ 23996-25-0 ]

[ 23996-25-0 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 23996-25-0 ]
  • 3-(2-ethyl-4-methyl-1H-imidazole-1-yl)-1-hydroxy-1-phosphonopropylphosphonic acid [ No CAS ]
  • 3
  • [ 23996-25-0 ]
  • C9H17N2O7P2(1-)*Na(1+) [ No CAS ]
  • 4
  • [ 931-36-2 ]
  • [ 107-13-1 ]
  • [ 23996-25-0 ]
YieldReaction ConditionsOperation in experiment
87% With C22H48N4(4+)*4HO(1-); In neat (no solvent); at 20℃; for 1.16667h; General procedure: alpha,beta-unsaturated compound (4.8 mmol) was added dropwise to a well stirred mixture of N-heterocycle substrate (4.0 mmol) in [n-butyl urotropinium]OH (0.108 g, 0.25 mmol) and the reaction mixture was stirred for required time until completion of reaction (TLC). The product was then directly distilled out from the reaction mixture to provide pure Michael adducts (3a-3f and 4a-4f) in high yields.
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