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[ CAS No. 50-30-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 50-30-6
Chemical Structure| 50-30-6
Structure of 50-30-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 50-30-6 ]

CAS No. :50-30-6 MDL No. :MFCD00002418
Formula : C7H4Cl2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MRUDNSFOFOQZDA-UHFFFAOYSA-N
M.W : 191.01 Pubchem ID :5758
Synonyms :
Chemical Name :2,6-Dichlorobenzoic acid

Calculated chemistry of [ 50-30-6 ]      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) : -5.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.44
Log Po/w (XLOGP3) : 2.23
Log Po/w (WLOGP) : 2.69
Log Po/w (MLOGP) : 2.79
Log Po/w (SILICOS-IT) : 2.5
Consensus Log Po/w : 2.33

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.77
Solubility : 0.327 mg/ml ; 0.00171 mol/l
Class : Soluble
Log S (Ali) : -2.65
Solubility : 0.429 mg/ml ; 0.00225 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 : 1.19

Safety of [ 50-30-6 ]

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

Application In Synthesis of [ 50-30-6 ]

* 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 [ 50-30-6 ]

[ 50-30-6 ] Synthesis Path-Downstream   1~3

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  • [ 50-30-6 ]
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  • [ 50-30-6 ]
  • [ 948895-18-9 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20℃; for 14h; Example 44; s 2,6-Dichloro-iV-[2-(4-[(2i?)-2-hydroxy-2-(8-hydroxy-2-oxo-l,2-dihydroquinolin-5- yl)ethyl]amino}piperidin-l-yl)ethyl]benzamide; i) 2,6-Dichloro-iV-[2-(4-hydroxypiperidin-l-yl)ethyl]benzamideA solution of l-(2-aminoethyl)piperidm-4-ol (0.312 g), 2,6-dichlorobenzoic acid (0.826g), 0 and triethylamine (0.61 mL) in DMF (10 mL) was treated with PyBROP (1.2Ig) at ambient temperature. After stirring for 14 h the mixture was loaded onto a SCX cartridge and eluted with acetonitrile followed by methanol. The product was then eluted off with ammonia/methanol solutions to give the subtitle compound, after solvent evaporation, as a yellow oil. Yield: 0.7g s MS APCI+ 317/319/321 [M+H]+
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  • [ 25185-95-9 ]
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