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[ CAS No. 143314-16-3 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 143314-16-3
Chemical Structure| 143314-16-3
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Product Citations

Product Citations

Zhao, Xiaolei ; Alsufyani, Maryam ; Tian, Junfu , et al. DOI: PubMed ID:

Abstract: Achieving efficient doping in n-type conjugated polymers is crucial for their application in electronic devices. In this study, an n-type doping method is developed based on cation exchange that maintains a high doping level while ensuring a high degree of structural order, leading to significantly improved electrical conductivity. By investigating various dopants and ionic liquids, it is discovered that the choice of dopant influences doping efficiency, while the selection of ionic liquid affects cation exchange efficiency. Through careful selection of suitable dopants and ionic liquids, High doping levels are achieved remarkably in a short period, resulting in the highest conductivity (nearly 1 × 10?2 S cm?1) compared to other doping methods for poly{[N,N′-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)} (N2200). The findings highlight the robustness and efficiency of cation exchange doping as an effective approach for achieving high-quality n-type doping in conjugated polymers, thereby opening new avenues for the development of advanced polymer-based electronic devices.

Keywords: cation exchange ; conjugated polymer ; electrical conductivity ; n-type doping

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Product Details of [ 143314-16-3 ]

CAS No. :143314-16-3 MDL No. :MFCD00216668
Formula : C6H11BF4N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CUNYTRQQXKCRTJ-UHFFFAOYSA-N
M.W : 197.97 Pubchem ID :2769348
Synonyms :

Calculated chemistry of [ 143314-16-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.5
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.28
TPSA : 8.81 ?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) : -5.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.66
Log Po/w (WLOGP) : 3.31
Log Po/w (MLOGP) : 1.0
Log Po/w (SILICOS-IT) : 0.26
Consensus Log Po/w : 1.45

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.96
Solubility : 0.216 mg/ml ; 0.00109 mol/l
Class : Soluble
Log S (Ali) : -2.5
Solubility : 0.631 mg/ml ; 0.00319 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.71
Solubility : 39.0 mg/ml ; 0.197 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.47

Safety of [ 143314-16-3 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P273-P280-P301+P310+P330-P302+P352-P305+P351+P338-P312-P332+P313-P337+P313-P391-P405-P501 UN#:2810
Hazard Statements:H301-H313-H315-H319-H411 Packing Group:
GHS Pictogram:
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