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[ CAS No. 4841-22-9 ] {[proInfo.proName]}

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Chemical Structure| 4841-22-9
Chemical Structure| 4841-22-9
Structure of 4841-22-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4841-22-9 ]

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Product Details of [ 4841-22-9 ]

CAS No. :4841-22-9 MDL No. :MFCD00063317
Formula : C9H9ClO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OSGZHKYFZSNKRI-UHFFFAOYSA-N
M.W : 200.62 Pubchem ID :96277
Synonyms :

Calculated chemistry of [ 4841-22-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 48.84
TPSA : 35.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.08 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.39
Log Po/w (XLOGP3) : 2.04
Log Po/w (WLOGP) : 1.89
Log Po/w (MLOGP) : 1.94
Log Po/w (SILICOS-IT) : 2.22
Consensus Log Po/w : 2.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.45
Solubility : 0.717 mg/ml ; 0.00358 mol/l
Class : Soluble
Log S (Ali) : -2.41
Solubility : 0.773 mg/ml ; 0.00385 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.24
Solubility : 0.115 mg/ml ; 0.000575 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.78

Safety of [ 4841-22-9 ]

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

Application In Synthesis of [ 4841-22-9 ]

* 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 [ 4841-22-9 ]

[ 4841-22-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4841-22-9 ]
  • [ 13730-98-8 ]
YieldReaction ConditionsOperation in experiment
209.15 g With sodium hydrogencarbonate; In water; at 80℃; for 2.0h; To the obtained methyl 4-chlorophenoxyacetate, 87.07 g of 99% sodium hydrogencarbonate and 129.30 g of water were added, and the mixture was reacted at 80 C for 2 h.At the same time, the alcohol formed by the reaction is distilled off, and the reaction is cooled down to room temperature for filtration.The filter cake is dried to obtain 209.15 g of sodium 4-chlorophenoxyacetate, and the content is 98.6%.The total yield was 98.86% based on phenol.
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