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[ CAS No. 56187-37-2 ] {[proInfo.proName]}

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Chemical Structure| 56187-37-2
Chemical Structure| 56187-37-2
Structure of 56187-37-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 56187-37-2 ]

CAS No. :56187-37-2 MDL No. :MFCD02180547
Formula : C7H5Cl2NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :MFMXEEQESUEMSB-UHFFFAOYSA-N
M.W : 222.03 Pubchem ID :92052
Synonyms :

Calculated chemistry of [ 56187-37-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.56
TPSA : 59.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.27
Log Po/w (XLOGP3) : 1.55
Log Po/w (WLOGP) : 1.24
Log Po/w (MLOGP) : 0.31
Log Po/w (SILICOS-IT) : 1.47
Consensus Log Po/w : 1.17

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.4
Solubility : 0.879 mg/ml ; 0.00396 mol/l
Class : Soluble
Log S (Ali) : -2.4
Solubility : 0.874 mg/ml ; 0.00394 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.12
Solubility : 1.66 mg/ml ; 0.0075 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.83

Safety of [ 56187-37-2 ]

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 [ 56187-37-2 ]

* 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 [ 56187-37-2 ]

[ 56187-37-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 56187-37-2 ]
  • [ 30246-33-4 ]
  • [ 56187-47-4 ]
YieldReaction ConditionsOperation in experiment
93% With ortho-iodophenylboronic acid; In toluene;Reflux; 200ml of toluene and 2-iodophenylboronic acid (0.21mol) were added to a clean reaction flask, then compound IV210.93g (1.06mol) was added, and then compound III327.21g (0.95mol) was slowly added, and the reaction was refluxed for 5-6h, After the reaction, cooled to room temperature, transferred to purified water, separated the solid and filtered, washed with purified water, recrystallized with ethanol, and dried under vacuum to obtain 484.55 g of cefoxidone (I), with a molar yield of 93% and a purity of 99.9 %,Maximum single impurity 0.04%
  • 2
  • [ 56187-37-2 ]
  • [ 56187-47-4 ]
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