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[ CAS No. 3457-45-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3457-45-2
Chemical Structure| 3457-45-2
Structure of 3457-45-2 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Surya R. Banks ; J. Tanner Morningstar ; Mark E. Welker DOI:

Abstract: A series of small molecules containing aminopropyltriethoxysilane (APTES) linkers were synthesized so that they could potentially be incorporated into self-assembled monolayers (SAMS) on metal oxide surfaces. Trialkoxysilanes are widely used to modify metal oxide surfaces since they readily react with surface hydroxyl groups to release the alkanol and provide a piano stool trialkoxysilane linkage to the surface [1,2,3,4,5,6,7,8,9,10,11]. Two main structural aspects of the small molecules to be synthesized were considered: (1) ease of synthesis of the small molecule, i.e., where possible, one-pot reactions from inexpensive, commercially available starting materials, and (2) presentation of a variety of aromatic functional groups that would be of interest to others working to use SAMS as components of materials for molecular electronics or sensing applications. Imines that contain both electron-donating and -withdrawing substituents on a benzene ring, as well as a number of imines with nitrogen heterocycles as the aromatic component, were prepared. Amides were prepared containing pyridine, furan, and thiophene rings as part of the aromatic component.

Keywords: aminopropyltriethoxysilane ; amide ; imine ; self-assembled monolayer

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Product Details of [ 3457-45-2 ]

CAS No. :3457-45-2 MDL No. :MFCD02093689
Formula : C9H8O2 Boiling Point : -
Linear Structure Formula :- InChI Key :KTFKRVMXIVSARW-UHFFFAOYSA-N
M.W : 148.16 Pubchem ID :5009465
Synonyms :

Calculated chemistry of [ 3457-45-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.11
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.02
TPSA : 34.14 ?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) : -6.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.33
Log Po/w (XLOGP3) : 0.97
Log Po/w (WLOGP) : 1.7
Log Po/w (MLOGP) : 1.08
Log Po/w (SILICOS-IT) : 2.32
Consensus Log Po/w : 1.48

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.64
Solubility : 3.38 mg/ml ; 0.0228 mol/l
Class : Very soluble
Log S (Ali) : -1.27
Solubility : 7.87 mg/ml ; 0.0531 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.66
Solubility : 0.323 mg/ml ; 0.00218 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 3457-45-2 ]

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

Application In Synthesis of [ 3457-45-2 ]

* 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 [ 3457-45-2 ]

[ 3457-45-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3457-45-2 ]
  • [ 62-53-3 ]
  • [ 446065-11-8 ]
  • 1-(4-(cyclohexyl(phenylamino)methyl)phenyl)ethan-1-one [ No CAS ]
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