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[ CAS No. 14527-43-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 14527-43-6
Chemical Structure| 14527-43-6
Structure of 14527-43-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 14527-43-6 ]

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Product Details of [ 14527-43-6 ]

CAS No. :14527-43-6 MDL No. :MFCD03788566
Formula : C6H7NO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :XDOKFEJMEJKVGX-UHFFFAOYSA-N
M.W : 157.19 Pubchem ID :5003096
Synonyms :

Calculated chemistry of [ 14527-43-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.33
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.2
TPSA : 67.43 ?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) : -6.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.86
Log Po/w (XLOGP3) : 1.51
Log Po/w (WLOGP) : 1.32
Log Po/w (MLOGP) : 0.02
Log Po/w (SILICOS-IT) : 2.19
Consensus Log Po/w : 1.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.94
Solubility : 1.81 mg/ml ; 0.0115 mol/l
Class : Very soluble
Log S (Ali) : -2.53
Solubility : 0.459 mg/ml ; 0.00292 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.76
Solubility : 2.72 mg/ml ; 0.0173 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.45

Safety of [ 14527-43-6 ]

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

Application In Synthesis of [ 14527-43-6 ]

* 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 [ 14527-43-6 ]

[ 14527-43-6 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 3973-08-8 ]
  • [ 64-17-5 ]
  • [ 14527-43-6 ]
YieldReaction ConditionsOperation in experiment
87.6% With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20℃; for 5h; General procedure: 2.5mmol thiazole-4-carboxyli acid and 2.0mmol alcohol were dissolved in 25mL dichloromethane (DCM) in a dry flask with continuous stirring, followed by the addition of 2.5mmol 3-(3-dimethylaminopropyl) -1-ethylcarbodiimide hydrochloride. When the temperature of the reaction system cooled to 0°C, 0.2mmol 4-dimethylaminopyridine was added dropwise and reacted for 1hat 0°C. Then the temperature was elevated to room temperature for another 4h reaction. The reaction was stopped by adding 25mL saturated NaHCO3 solution and extracted twice with 20mL dichloromethane (2×20mL). The extracted organic layers were first dried by anhydrous Na2SO4, and then filtered and concentrated under vacuum distillation, obtaining the crude products. Finally, the crude products were further purified using column chromatography (ethy lacetate:petroleum ether, 1:5).
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