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[ CAS No. 2213-63-0 ] {[proInfo.proName]}

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Chemical Structure| 2213-63-0
Chemical Structure| 2213-63-0
Structure of 2213-63-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2213-63-0 ]

CAS No. :2213-63-0 MDL No. :MFCD00006720
Formula : C8H4Cl2N2 Boiling Point : -
Linear Structure Formula :- InChI Key :SPSSDDOTEZKOOV-UHFFFAOYSA-N
M.W : 199.04 Pubchem ID :16659
Synonyms :

Calculated chemistry of [ 2213-63-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.56
TPSA : 25.78 ?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) : -5.38 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.17
Log Po/w (XLOGP3) : 3.0
Log Po/w (WLOGP) : 2.94
Log Po/w (MLOGP) : 2.03
Log Po/w (SILICOS-IT) : 3.21
Consensus Log Po/w : 2.67

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.58
Solubility : 0.0523 mg/ml ; 0.000263 mol/l
Class : Soluble
Log S (Ali) : -3.21
Solubility : 0.124 mg/ml ; 0.000623 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.57
Solubility : 0.00542 mg/ml ; 0.0000272 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.75

Safety of [ 2213-63-0 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P301+P310+P330-P302+P352-P305+P351+P338 UN#:2811
Hazard Statements:H301-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2213-63-0 ]

* 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 [ 2213-63-0 ]

[ 2213-63-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2213-63-0 ]
  • [ 18628-07-4 ]
  • C32H19ClN4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
94% With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20℃; for 1h; After introducing compound 2-1 (15.1 g, 45.4 mmol), sodium hydride (60%) (2.2 g, 54.5 mmol), 1,2-dichloroquinoxaline (10.8 g, 54.5 mmol), and DMF (200 mL) into a flask, the mixture was stirred at room temperature for 1 hour. Methanol and purified water were added to the mixture to obtain a solid substance. The solid substance was filtered, and dried under reduced pressure to obtain compound 2-2 (21 g, 94 %).
94% With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20℃; for 1h; Compound 2-1(15.1 g, 45.4 mmol),NaH (60% in mineral oil)(2.2 g, 54.5 mmol),2,3-Dichloroquinoxaline (10.8 g, 54.5 mmol)And 200 mL of DMF were added, and the mixture was stirred at room temperature for 1 hour.Methanol and purified water were added to produce a solid. The solid was filtered and dried under reduced pressure to obtain Compound 2-2 (21 g, yield: 94%).
  • 2
  • [ 2213-63-0 ]
  • [ 10241-97-1 ]
  • C18H11N3O2 [ No CAS ]
  • 3
  • [ 2213-63-0 ]
  • [ 32566-01-1 ]
  • 5,10-dihydrobenzo[6,7]indolo[3′,2′:4,5]azepino[2,3-b]quinoxaline [ No CAS ]
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