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[ CAS No. 181219-01-2 ] {[proInfo.proName]}

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Chemical Structure| 181219-01-2
Chemical Structure| 181219-01-2
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Product Details of [ 181219-01-2 ]

CAS No. :181219-01-2 MDL No. :MFCD01319051
Formula : C11H16BNO2 Boiling Point : -
Linear Structure Formula :NC5H4BOC(CH3)2C(CH3)2O InChI Key :NLTIETZTDSJANS-UHFFFAOYSA-N
M.W : 205.06 Pubchem ID :2734648
Synonyms :
Chemical Name :4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Calculated chemistry of [ 181219-01-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.55
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 60.71
TPSA : 31.35 ?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 : Yes
Log Kp (skin permeation) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.84
Log Po/w (WLOGP) : 1.38
Log Po/w (MLOGP) : 0.58
Log Po/w (SILICOS-IT) : 1.31
Consensus Log Po/w : 1.02

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.5
Solubility : 0.648 mg/ml ; 0.00316 mol/l
Class : Soluble
Log S (Ali) : -2.12
Solubility : 1.56 mg/ml ; 0.0076 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.63
Solubility : 0.0481 mg/ml ; 0.000234 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.61

Safety of [ 181219-01-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 181219-01-2 ]

* 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.

  • Upstream synthesis route of [ 181219-01-2 ]
  • Downstream synthetic route of [ 181219-01-2 ]

[ 181219-01-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 181219-01-2 ]
  • [ 81660-73-3 ]
Reference: [1] Green Chemistry, 2015, vol. 17, # 6, p. 3540 - 3551
[2] Organic Letters, 2014, vol. 16, # 7, p. 1836 - 1839
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