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[ CAS No. 58328-39-5 ] {[proInfo.proName]}

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Chemical Structure| 58328-39-5
Chemical Structure| 58328-39-5
Structure of 58328-39-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 58328-39-5 ]

CAS No. :58328-39-5 MDL No. :MFCD03095029
Formula : C8H7BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :NGOZRIZXELGVHK-UHFFFAOYSA-N
M.W : 215.04 Pubchem ID :18787268
Synonyms :

Calculated chemistry of [ 58328-39-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.01
TPSA : 18.46 ?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) : -5.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.35
Log Po/w (XLOGP3) : 2.33
Log Po/w (WLOGP) : 2.22
Log Po/w (MLOGP) : 1.83
Log Po/w (SILICOS-IT) : 2.85
Consensus Log Po/w : 2.31

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.04
Solubility : 0.194 mg/ml ; 0.000902 mol/l
Class : Soluble
Log S (Ali) : -2.36
Solubility : 0.946 mg/ml ; 0.0044 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.29
Solubility : 0.111 mg/ml ; 0.000515 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.33

Safety of [ 58328-39-5 ]

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

Application In Synthesis of [ 58328-39-5 ]

* 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 [ 58328-39-5 ]

[ 58328-39-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14381-51-2 ]
  • [ 106-93-4 ]
  • [ 58328-39-5 ]
YieldReaction ConditionsOperation in experiment
45% With potassium fluoride; In DMF (N,N-dimethyl-formamide); at 135℃; for 3h; To <strong>[14381-51-2]2,3-dihydroxy-bromobenzene</strong> (3.0 g, 0.16 mole), KF (4.63 g, 0.080 mole), DMF (15 ML was added CH2Br2 (4.13 g, 0.024 moles).. This suspension was heated to 135° C. for 3 hours, cooled and filtered.. The filtrate was poured into 200 ML of ether and washed with water, 1 N KOH and brine.. The organic layer was dried over magnesium sulfate, filtered and the solvent removed under vacuum, to yield 2,3-Methylenedioxy-bromobenzene (1.45 g, 45 percent yield).
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