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[ CAS No. 348-60-7 ] {[proInfo.proName]}

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Chemical Structure| 348-60-7
Chemical Structure| 348-60-7
Structure of 348-60-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 348-60-7 ]

CAS No. :348-60-7 MDL No. :MFCD00042583
Formula : C6H4ClFO Boiling Point : No data available
Linear Structure Formula :- InChI Key :XLHYAEBESNFTCA-UHFFFAOYSA-N
M.W : 146.55 Pubchem ID :2724523
Synonyms :

Calculated chemistry of [ 348-60-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 33.43
TPSA : 20.23 ?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) : -5.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.54
Log Po/w (XLOGP3) : 2.8
Log Po/w (WLOGP) : 2.6
Log Po/w (MLOGP) : 2.51
Log Po/w (SILICOS-IT) : 2.45
Consensus Log Po/w : 2.38

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.01
Solubility : 0.145 mg/ml ; 0.000986 mol/l
Class : Soluble
Log S (Ali) : -2.88
Solubility : 0.192 mg/ml ; 0.00131 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.7
Solubility : 0.295 mg/ml ; 0.00201 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.25

Safety of [ 348-60-7 ]

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

Application In Synthesis of [ 348-60-7 ]

* 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 [ 348-60-7 ]

[ 348-60-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 348-60-7 ]
  • [ 33742-70-0 ]
  • 6-(4-chloro-3-fluorophenoxy)-N-methyl-3-nitropyridin-2-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% With sodium hydride; In N,N-dimethyl-formamide; at 80℃; for 10.0h;Inert atmosphere; General procedure: NaH (12.0mmol) was added to a solution of 1 or 722 (1.88g, 10.0mmol) and substituted phenol (12.0mmol) in DMF (50mL) at room temperature under N2, and the mixture was stirred at 80C for 10h. Water was added to the cooled mixture, and the mixture was extracted with EtOAc several times. The combined organic layers were washed with water, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The crude residue was purified by silica gel column chromatography to obtain purified compound 2, or crude 2 was used directly for the next reaction without further purification.
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