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[ CAS No. 183803-12-5 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 183803-12-5
Chemical Structure| 183803-12-5
Chemical Structure| 183803-12-5
Structure of 183803-12-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 183803-12-5 ]

CAS No. :183803-12-5 MDL No. :MFCD16038723
Formula : C6H3BrCl2O Boiling Point : -
Linear Structure Formula :- InChI Key :LZEBXZCABIQUQF-UHFFFAOYSA-N
M.W : 241.90 Pubchem ID :19607720
Synonyms :

Calculated chemistry of [ 183803-12-5 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.19
TPSA : 20.23 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.12
Log Po/w (XLOGP3) : 3.78
Log Po/w (WLOGP) : 3.46
Log Po/w (MLOGP) : 3.41
Log Po/w (SILICOS-IT) : 3.34
Consensus Log Po/w : 3.22

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.17
Solubility : 0.0165 mg/ml ; 0.0000684 mol/l
Class : Moderately soluble
Log S (Ali) : -3.9
Solubility : 0.0306 mg/ml ; 0.000126 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.91
Solubility : 0.0296 mg/ml ; 0.000122 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.85

Safety of [ 183803-12-5 ]

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

Application In Synthesis of [ 183803-12-5 ]

* 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 [ 183803-12-5 ]

[ 183803-12-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 183803-12-5 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
10 Stage C: methyl (5-bromo 2,4-dichloro phenoxy) acetate Stage C: methyl (5-bromo 2,4-dichloro phenoxy) acetate The product was obtained from 5-bromo 2,4-dichloro phenol by operating as in Stage B of the starting product of Examples 1 and 2.
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