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[ CAS No. 193978-23-3 ] {[proInfo.proName]}

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Chemical Structure| 193978-23-3
Chemical Structure| 193978-23-3
Structure of 193978-23-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 193978-23-3 ]

CAS No. :193978-23-3 MDL No. :MFCD05663878
Formula : C10H15BO2S Boiling Point : No data available
Linear Structure Formula :C4H3SBO2C2(CH3)4 InChI Key :FFZHICFAHSDFKZ-UHFFFAOYSA-N
M.W : 210.10 Pubchem ID :10703628
Synonyms :
Chemical Name :4,4,5,5-Tetramethyl-2-(2-thienyl)-1,3,2-dioxaborolane

Calculated chemistry of [ 193978-23-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.6
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 60.8
TPSA : 46.7 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.62
Log Po/w (WLOGP) : 2.05
Log Po/w (MLOGP) : 1.22
Log Po/w (SILICOS-IT) : 2.5
Consensus Log Po/w : 1.68

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.99
Solubility : 0.214 mg/ml ; 0.00102 mol/l
Class : Soluble
Log S (Ali) : -3.25
Solubility : 0.118 mg/ml ; 0.000561 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.27
Solubility : 0.112 mg/ml ; 0.000535 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.18

Safety of [ 193978-23-3 ]

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

Application In Synthesis of [ 193978-23-3 ]

* 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.

  • Upstream synthesis route of [ 193978-23-3 ]
  • Downstream synthetic route of [ 193978-23-3 ]

[ 193978-23-3 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 589-87-7 ]
  • [ 193978-23-3 ]
  • [ 40133-22-0 ]
YieldReaction ConditionsOperation in experiment
74.6% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In tetrahydrofuran; water; toluene for 5 h; Reflux A mixture of 1-bromo-4-iodobenzene (2.0 g, 7.07 mmol), 4,4,5,5-tetramethyl-2-(thiophen-2-yl)-1,3,2-dioxaborolane (2.97 g, 14.1 mmol), Pd(PPh34 (408 mg, 0.35 mmol), and Na2CO3 (1.49 g, 14.1 mmol) were dissolved in toluene (40 mL), THF (15 mL), and H2O (15 mL) and the reaction mixture was refluxed for 5 h. After completion of the reaction (indicated by TLC), the solvent was removed under vacuum, H2O (30 mL) and CH2Cl2 (40 mL) were added. The organic layer was separated and dried on anhydrous MgSO4. The solvent was removed under reduced pressure. Then the crude product was purified by flash column chromatography on silica gel to give 2-(4-bromophenyl) thiophene (1.26 g, 74.6percent). Spectral data matched well with values reported in the literature.27 1HNMR (400 MHz, CDCl3: 7.48 (d, 3.6 Hz, 4 H), 7.29(d, 4.4 Hz, 2 H), 7.07 (dt, 1.4, 4.4 Hz, 1 H).
Reference: [1] Journal of Nanoscience and Nanotechnology, 2016, vol. 16, # 1, p. 910 - 919
[2] ChemPlusChem, 2017, vol. 82, # 5, p. 742 - 749
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