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[ CAS No. 2589-11-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2589-11-9
Chemical Structure| 2589-11-9
Structure of 2589-11-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2589-11-9 ]

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Product Details of [ 2589-11-9 ]

CAS No. :2589-11-9 MDL No. :MFCD12022343
Formula : C6H4ClN3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :GDXABUJCXZZPBI-UHFFFAOYSA-N
M.W : 153.57 Pubchem ID :21813895
Synonyms :

Calculated chemistry of [ 2589-11-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.9
TPSA : 41.57 ?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) : -6.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.96
Log Po/w (XLOGP3) : 1.38
Log Po/w (WLOGP) : 1.61
Log Po/w (MLOGP) : 0.37
Log Po/w (SILICOS-IT) : 2.24
Consensus Log Po/w : 1.31

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.33
Solubility : 0.722 mg/ml ; 0.0047 mol/l
Class : Soluble
Log S (Ali) : -1.86
Solubility : 2.14 mg/ml ; 0.0139 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.14
Solubility : 0.112 mg/ml ; 0.000728 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.67

Safety of [ 2589-11-9 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2589-11-9 ]

* 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 [ 2589-11-9 ]

[ 2589-11-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 64-18-6 ]
  • [ 2604-39-9 ]
  • [ 2589-11-9 ]
  • 2
  • [ 2604-39-9 ]
  • [ 122-51-0 ]
  • [ 2589-11-9 ]
  • 3
  • [ 2604-39-9 ]
  • [ 2589-11-9 ]
  • 4
  • [ 558-42-9 ]
  • [ 2589-11-9 ]
  • C10H12ClN3O [ No CAS ]
YieldReaction ConditionsOperation in experiment
34 mg With potassium carbonate; In acetonitrile; at 80℃; for 16h; 6-chloro-3H-imidazo [4,5-c] pyridine (100 mg), 1-chloro-2-methyl-2-propanol (200 muL)A mixture of potassium carbonate (135 mg) and acetonitrile (2 mL)Followed by stirring at 80 ° C. for 16 hours. After cooling to room temperature, the reaction solution was charged on silica gel and purified by silica gel column chromatography (eluent: chloroform / methanol = 10/1) to prepare compound 9 (34 mg).
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