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[ CAS No. 101861-63-6 ] {[proInfo.proName]}

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Chemical Structure| 101861-63-6
Chemical Structure| 101861-63-6
Structure of 101861-63-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 101861-63-6 ]

CAS No. :101861-63-6 MDL No. :MFCD00209870
Formula : C9H5Cl2NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :DHXISZKSSIWRLH-UHFFFAOYSA-N
M.W : 230.05 Pubchem ID :127988
Synonyms :

Calculated chemistry of [ 101861-63-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 55.28
TPSA : 53.09 ?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) : -5.46 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 3.16
Log Po/w (WLOGP) : 3.17
Log Po/w (MLOGP) : 2.21
Log Po/w (SILICOS-IT) : 3.14
Consensus Log Po/w : 2.65

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.67
Solubility : 0.0495 mg/ml ; 0.000215 mol/l
Class : Soluble
Log S (Ali) : -3.95
Solubility : 0.0261 mg/ml ; 0.000113 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.9
Solubility : 0.0292 mg/ml ; 0.000127 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.54

Safety of [ 101861-63-6 ]

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

Application In Synthesis of [ 101861-63-6 ]

* 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 [ 101861-63-6 ]

[ 101861-63-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 101861-63-6 ]
  • [ 101495-18-5 ]
YieldReaction ConditionsOperation in experiment
14 g With copper dichloride; In dimethyl sulfoxide; at 120.0℃; for 1.0h; In the reaction bottle,22 g of 4,6-dichloroindolecarboxylic acid was added to 150 mL of DMSO, and then 3 g of copper chloride was added.The reaction was heated at 120 C for 1 h,TLC monitors the reaction of the starting material completely, and the reaction solution is filtered, and then 200 mL of dichloromethane is added to extract the reaction solution three times.The organic phases were combined, washed with 200 mL of water and concentrated.Then in a mixture of acetone and n-hexane (V acetone: V-hexane = 3:1)Recrystallization from 100 mL gives 4,6-dichloroanthracene 14g
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