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[ CAS No. 97229-11-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 97229-11-3
Chemical Structure| 97229-11-3
Structure of 97229-11-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 97229-11-3 ]

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Product Details of [ 97229-11-3 ]

CAS No. :97229-11-3 MDL No. :MFCD09701372
Formula : C5H5ClN2O2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :BWVZLXTZQHILRC-UHFFFAOYSA-N
M.W : 192.62 Pubchem ID :11148232
Synonyms :

Calculated chemistry of [ 97229-11-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.14
TPSA : 68.3 ?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) : -6.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.1
Log Po/w (XLOGP3) : 0.74
Log Po/w (WLOGP) : 1.61
Log Po/w (MLOGP) : -0.29
Log Po/w (SILICOS-IT) : 0.9
Consensus Log Po/w : 0.81

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.84
Solubility : 2.8 mg/ml ; 0.0145 mol/l
Class : Very soluble
Log S (Ali) : -1.75
Solubility : 3.4 mg/ml ; 0.0176 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.58
Solubility : 0.502 mg/ml ; 0.00261 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.91

Safety of [ 97229-11-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 97229-11-3 ]

* 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 [ 97229-11-3 ]

[ 97229-11-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 97229-11-3 ]
  • [ 56456-49-6 ]
  • 4-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]pyrimidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
54% With sodium hydride; In tetrahydrofuran; mineral oil; at -25 - 25℃; for 18.5h; This reaction was carried out in two identical batches. A solution of (4-chloro-2- fluorophenyl)methanol (5.42 g, 33.8 mmol) in THF (60 ml_) was added drop-wise, over a period of 25 minutes, to a -25 C suspension of 4-chloro-2-(methylsulfonyl)pyrimidine (13.0 g, 67.5 mmol) and sodium hydride (60% dispersion in mineral oil; 2.43 g, 60.8 mmol) in THF (180 ml_). The reaction mixture was allowed to stir at room temperature (25 C) for 18 hours, whereupon the two batches were combined and concentrated in vacuo. The residue was diluted with saturated aqueous ammonium chloride solution (120 ml_) and extracted with EtOAc (3 x 100 ml_); the combined organic layers were dried over sodium sulfate, filtered, concentrated under reduced pressure, and purified via silica gel chromatography (Gradient: 0% to 6% EtOAc in petroleum ether), affording P8 as a white solid. Combined yield: 9.93 g, 36.4 mmol, 54%. LCMS m/z 272.7 (dichloro isotope pattern observed) [M+H]+. 1H NMR (400 MHz, Chloroform-d) 5 8.41 (d, 1 H), 7.48 (dd, 1 H), 7.17 - 7.10 (m, 2H), 7.02 (d, 1 H), 5.46 (s, 2H).
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