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[ CAS No. 50-79-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 50-79-3
Chemical Structure| 50-79-3
Structure of 50-79-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 50-79-3 ]

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Product Details of [ 50-79-3 ]

CAS No. :50-79-3 MDL No. :MFCD00002416
Formula : C7H4Cl2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :QVTQYSFCFOGITD-UHFFFAOYSA-N
M.W : 191.01 Pubchem ID :5784
Synonyms :

Calculated chemistry of [ 50-79-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.42
TPSA : 37.3 ?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) : -5.46 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.52
Log Po/w (XLOGP3) : 2.82
Log Po/w (WLOGP) : 2.69
Log Po/w (MLOGP) : 2.79
Log Po/w (SILICOS-IT) : 2.5
Consensus Log Po/w : 2.46

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.14
Solubility : 0.139 mg/ml ; 0.000727 mol/l
Class : Soluble
Log S (Ali) : -3.26
Solubility : 0.105 mg/ml ; 0.000549 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.01
Solubility : 0.188 mg/ml ; 0.000986 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.26

Safety of [ 50-79-3 ]

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 [ 50-79-3 ]

* 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 [ 50-79-3 ]

[ 50-79-3 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 16611-67-9 ]
  • KMnO4 [ No CAS ]
  • aqueous NaOH [ No CAS ]
  • [ 50-79-3 ]
  • 2
  • [ 54396-44-0 ]
  • [ 12775-96-1 ]
  • [ 50-79-3 ]
  • [ 61708-30-3 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In pentan-1-ol; EXAMPLE 4 5-Chloro-N-(2-methyl-3-trifluoromethylphenyl) anthranilic acid To a solution of 25 g. of 2,5-dichlorobenzoic acid in 125 ml. of n-pentyl alcohol add 4.8 g. of sodium hydroxide pellets, 25 g. of <strong>[54396-44-0]2-methyl-3-trifluoromethylaniline</strong> and 2 g. of copper powder. With constant stirring, reflux the reaction mixture for 18 hours. Concentrate the mixture to one half volume and dilute with water and ether. Acidify the aqueous layer to yield the product which is recrystallized from methanol, m.p. 220°-222° C.
  • 3
  • [ 50-79-3 ]
  • [ 16611-67-9 ]
  • 4
  • [ 245660-15-5 ]
  • [ 50-79-3 ]
  • C17H28ClNO3Si [ No CAS ]
YieldReaction ConditionsOperation in experiment
With copper(I) oxide; copper; potassium carbonate; In 1,2-dimethoxyethane; at 100℃; for 1.5h; A mixture of 38a (532.4 mg, 2.62 mmol), 2-5-dichlorobenzoic acid (250 mg, 1 .309 mmol, Aldrich), potassium carbonate (180.9 mg, 1.309 mmol), copper powder (8.3 mg, 0.131 mmol) and copper(l) oxide (9.4 mg, 0.065 mmol) in DME (3 mL) is heated to 100C for 1 .5 hours. The mixture is cooled to RT, and water is added. The mixture is neutralized with HCI 1 N until slightly acidic (pH 5-6) and then extracted with EtOAc (3x). The organic layers are combined, washed with water (2x), NH4CI saturated (2x) and brine, dried over MgSO4, filtered and concentrated. The residue is purified by Combif lash (Hex/EtOAc 100:0 to 70:30) to afford 38b.
  • 6
  • [ 50-79-3 ]
  • [ 1201902-80-8 ]
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