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[ CAS No. 16116-78-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 16116-78-2
Chemical Structure| 16116-78-2
Structure of 16116-78-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 16116-78-2 ]

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Product Details of [ 16116-78-2 ]

CAS No. :16116-78-2 MDL No. :MFCD01863556
Formula : C11H13BrSi Boiling Point : No data available
Linear Structure Formula :BrC6H4CCSi(CH3)3 InChI Key :RNMSGCJGNJYDNS-UHFFFAOYSA-N
M.W : 253.21 Pubchem ID :4226980
Synonyms :

Calculated chemistry of [ 16116-78-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.27
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 64.37
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.42
Log Po/w (XLOGP3) : 4.81
Log Po/w (WLOGP) : 3.76
Log Po/w (MLOGP) : 4.45
Log Po/w (SILICOS-IT) : 2.55
Consensus Log Po/w : 3.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.78
Solubility : 0.00419 mg/ml ; 0.0000165 mol/l
Class : Moderately soluble
Log S (Ali) : -4.54
Solubility : 0.00726 mg/ml ; 0.0000287 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.6
Solubility : 0.00633 mg/ml ; 0.000025 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.51

Safety of [ 16116-78-2 ]

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 [ 16116-78-2 ]

* 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 [ 16116-78-2 ]

[ 16116-78-2 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 16116-78-2 ]
  • [ 630127-51-4 ]
  • 2
  • [ 16116-78-2 ]
  • [ 111291-97-5 ]
  • C24H26O2Si [ No CAS ]
  • 3
  • [ 39604-97-2 ]
  • [ 16116-78-2 ]
  • C22H24OSi [ No CAS ]
  • 4
  • [ 1202-25-1 ]
  • [ 16116-78-2 ]
  • 4,4'-bis(trimethylsilylethynyl)-4''-dimethylaminotriphenylmethanol [ No CAS ]
  • 5
  • [ 1202-25-1 ]
  • [ 16116-78-2 ]
  • 4,4'-diethynyl-4''-dimethylaminotriphenylmethanol [ No CAS ]
  • 6
  • [ 591-50-4 ]
  • [ 16116-78-2 ]
  • [ 13667-12-4 ]
YieldReaction ConditionsOperation in experiment
399 mg With water; 1,8-diazabicyclo[5.4.0]undec-7-ene; at 20℃; for 30h;Inert atmosphere; Schlenk technique; PdCl2(PPh3)2 (84 mg, 0.12 mmol,6.0 mol%), CuI (38 mg, 0.20 mmol, 10 mol%) and 1-bromo-4-iodobenzene (566 mg,2.0 mmol, 1.0 equiv) were added into a 30-mL 2-neck round-bottom flask with amagnetic stirring bar. The flask was evacuated and refilled with N2 gas following theusual Schlenk technique. Dry benzene (10 mL) was added while stirring. N2-spargedNEt3 (1.7 mL, 12 mmol, 6.0 equiv) and trimethylsilylacetylene (0.28 mL, 2.0 mmol,1.0 equiv) were added and the reaction flask was wrapped with aluminum foil andstirred at room temperature for 18 h. Iodobenzene (408 mg, 2.0 mmol, 1.0 equiv),DBU (3.6 mL, 24 mmol, 12.0 equiv) and distilled water (14 μL, 0.8 mmol, 40 mol%)were added consecutively and stirring was continued at room temperature foradditional 30 h. The reaction was quenched with water (10 mL) and extracted withdiethyl ether (10 mL). The organic layer was washed with 10% aqueous HCl (3 10mL), brine (20 mL), dried over Na2SO4, gravity-filtered and the solvent removed invacuo. The crude product was purified by silica gel column chromatography inhexane and concentrated in vacuo to obtain 1h in 78% (399 mg, 1.6 mmol) yield ascrystals.
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