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[ CAS No. 23228-45-7 ] {[proInfo.proName]}

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Chemical Structure| 23228-45-7
Chemical Structure| 23228-45-7
Structure of 23228-45-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 23228-45-7 ]

CAS No. :23228-45-7 MDL No. :MFCD06208178
Formula : C8H4ClF3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :DTIJZEUKFYGSEC-UHFFFAOYSA-N
M.W : 224.56 Pubchem ID :11118363
Synonyms :

Calculated chemistry of [ 23228-45-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.41
TPSA : 37.3 ?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) : -4.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.57
Log Po/w (XLOGP3) : 3.94
Log Po/w (WLOGP) : 4.21
Log Po/w (MLOGP) : 3.24
Log Po/w (SILICOS-IT) : 2.91
Consensus Log Po/w : 3.17

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.9
Solubility : 0.0283 mg/ml ; 0.000126 mol/l
Class : Soluble
Log S (Ali) : -4.42
Solubility : 0.00848 mg/ml ; 0.0000378 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -3.28
Solubility : 0.118 mg/ml ; 0.000524 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.53

Safety of [ 23228-45-7 ]

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 [ 23228-45-7 ]

* 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 [ 23228-45-7 ]

[ 23228-45-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 23228-45-7 ]
  • [ 56456-51-0 ]
YieldReaction ConditionsOperation in experiment
96% With borane-THF; at 0 - 30℃; for 1h; To a IN solution of borane in tetrahydrofuran (30 ml) was added 2-chloro-4-trifluoromethylbenzoic acid (2.50 g) , and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into IN hydrochloric acid, and the mixture was extracted with, ethyl acetate . The extract was washed with an aqueous sodium hydrogencarbonate solution and saturated 0 brine, dried (MgSO4) , and concentrated. The residue was subjected to silica gel column chromatography, and eluted with ethyl acetate-hexane (1:24 - 1:4, v/v) to give 2-chloro-4- trifluoromethylbenzyl alcohol (2.23 g, yield: 96%) as a colorless oil. 5 1H-NMR (300 MHz, CDCl3) delta:4.85 (2 H, d, J = 9.0 Hz), 7.52 - EPO <DP n="167"/>7 . 80 ( 3 H, m) .
96% With borane; In tetrahydrofuran; Reference Example 129 To a 1N solution (30 ml) of borane in tetrahydrofuran was added 2-chloro-4-(trifluoromethyl)benzoic acid (2.50 g), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was washed with aqueous sodium hydrogencarbonate and saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:24 to 1:4, v/v) to give 2-chloro-4-(trifluoromethyl)benzyl alcohol (2.23 g, yield 96%) as a colorless oil. 1H-NMR (300 MHz, CDCl3) delta:4.85 (2 H, d, J = 9.0 Hz), 7.52 - 7.80 (3 H, m).
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