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[ CAS No. 16588-16-2 ] {[proInfo.proName]}

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Chemical Structure| 16588-16-2
Chemical Structure| 16588-16-2
Structure of 16588-16-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 16588-16-2 ]

CAS No. :16588-16-2 MDL No. :MFCD00219621
Formula : C9H8ClNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :BLNLZRQIUGDTAO-UHFFFAOYSA-N
M.W : 229.62 Pubchem ID :1268247
Synonyms :

Calculated chemistry of [ 16588-16-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 56.36
TPSA : 72.12 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.93
Log Po/w (XLOGP3) : 2.68
Log Po/w (WLOGP) : 2.42
Log Po/w (MLOGP) : 1.73
Log Po/w (SILICOS-IT) : 0.57
Consensus Log Po/w : 1.87

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.98
Solubility : 0.238 mg/ml ; 0.00104 mol/l
Class : Soluble
Log S (Ali) : -3.85
Solubility : 0.0327 mg/ml ; 0.000142 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.88
Solubility : 0.301 mg/ml ; 0.00131 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 16588-16-2 ]

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 [ 16588-16-2 ]

* 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 [ 16588-16-2 ]

[ 16588-16-2 ] Synthesis Path-Downstream   1~3

  • 3
  • [ 1006-67-3 ]
  • [ 16588-16-2 ]
  • [ 118938-24-2 ]
YieldReaction ConditionsOperation in experiment
94.6% With potassium carbonate; dimethyl sulfoxide; EXAMPLE 20 Synthesis of Compound (50), 5-phenyl-(4-ethoxycarbonyl-2-nitrophenyl)-4-isoxazolin-3-one: After mixing 200 g of ethyl 4-chloro-3-nitrobenzoate, 500 ml of dimethyl sulfoxide, 169 g of <strong>[1006-67-3]5-phenylisoxazole</strong>, and 146 g of potassium carbonate, the reaction was performed for 5 hours at 60 C. After the reaction was over, the reaction mixture was cooled and poured into water to deposit crystals which were then recovered, washed with water, and dried to provide 292 g of the desired product with a yield of 94.6%. The melting point thereof was 142 C. to 143 C.
94.6% With potassium carbonate; dimethyl sulfoxide; Synthesis Example 12-1 Synthesis of 5-phenyl-(4-ethoxycarbonyl-2-nitrophenyl)-4-isoxazolin-3-one After mixing 200 g of ethyl 4-chloro-3-nitrobenzoate, 500 ml of dimethyl sulfoxide, 169 g of <strong>[1006-67-3]5-phenylisoxazole</strong>, and 146 g of potassium carbonate, the reaction was performed for 5 hours at 60 C. After the reaction was over, the reaction mixture was cooled and poured into water. Crystals thus deposited were recovered by filtration, washed with water, and dried to provide 292 g of the above-described compound with a yield of 94.6%. The melting point thereof was 142 C. to 143 C.
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