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[ CAS No. 2495-35-4 ] {[proInfo.proName]}

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Chemical Structure| 2495-35-4
Chemical Structure| 2495-35-4
Structure of 2495-35-4 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Wuyang Huang ; Kiho Cho ; Martina Stenzel , et al. DOI:

Abstract: The interfacial adhesions between inorganic short glass fibres and organic PEEK matrix play a crucial role in the mechanical properties of short glass fiber reinforced PEEK (SGFR-PEEK) bio-composites, while the inherent chemical inertness of PEEK imposes great challenges on the fibre-matrix interfacial modifications. In this experimental investigation, the effects of monomer/polymer selection, chemical concentration, UV-modification time on the thermal, mechanical properties and surface wettability of SGFR-PEEK composites were experimentally studied for the first time. The photo-polymerisation effectively modified the chemical structure, surface wettability of SGFR-PEEK composites and caused significant improvements on the tensile modulus (up to 16.35%) and flexural modulus (up to 11.63%) of SGFR-PEEK composites without noticable decrement on thermal properties, manifesting great potential and advantages for the developments of high-performance bio-composites.

Keywords: PEEK ; short S-Glass fibre ; UV-modification ; fibre-matrix interfacial adhesion ; mechanical properties ; surface wettability

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Product Details of [ 2495-35-4 ]

CAS No. :2495-35-4 MDL No. :MFCD00048147
Formula : C10H10O2 Boiling Point : No data available
Linear Structure Formula :CH2CHCO(OCH2C6H5) InChI Key :GCTPMLUUWLLESL-UHFFFAOYSA-N
M.W : 162.19 Pubchem ID :75617
Synonyms :

Calculated chemistry of [ 2495-35-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.1
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.64
TPSA : 26.3 ?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) : -5.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.29
Log Po/w (XLOGP3) : 2.55
Log Po/w (WLOGP) : 1.76
Log Po/w (MLOGP) : 2.2
Log Po/w (SILICOS-IT) : 2.37
Consensus Log Po/w : 2.23

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.56
Solubility : 0.449 mg/ml ; 0.00277 mol/l
Class : Soluble
Log S (Ali) : -2.75
Solubility : 0.289 mg/ml ; 0.00178 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.93
Solubility : 0.192 mg/ml ; 0.00118 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.43

Safety of [ 2495-35-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P273-P280-P302+P352-P304+P340-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2495-35-4 ]

* 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 [ 2495-35-4 ]

[ 2495-35-4 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 186581-53-3 ]
  • [ 2495-35-4 ]
  • [ 2409-87-2 ]
  • [ 4336-20-3 ]
  • [ 62638-06-6 ]
  • 2
  • [ 2495-35-4 ]
  • [ 255735-88-7 ]
  • [ 851017-82-8 ]
  • 3
  • [ 7446-81-3 ]
  • [ 100-44-7 ]
  • [ 2495-35-4 ]
YieldReaction ConditionsOperation in experiment
85.0%Chromat. Aliquat 336; sodium iodide; In water; at 50℃; for 2.5h; In Example 8, benzyl acrylate was prepared by dissolving <strong>[7446-81-3]sodium acrylate</strong> (10 mmoles = 0.95 g) in water (101.3 g). The reaction flask was immersed in the water bath at 50°C and magnetically stirred. Then, a mixture consisting of benzyl chloride (50 mmoles = 6.29 g), Aliquat 336 (2 mmoles = 0.85 g), and sodium iodide (2 mmoles = 0.30 g) was added to the water phase. The reaction mixture was stirred magnetically at 50°C. The reaction mixture after 150 minutes consisted of benzyl acrylate in a 85.0percent theoretical yield based on <strong>[7446-81-3]sodium acrylate</strong>. Analysis was done with an external standard of Durene (tetramethylbenzene) on a Gas Chromatograph.
  • 4
  • [ 2495-35-4 ]
  • [ 621-63-6 ]
  • [ 1046492-63-0 ]
YieldReaction ConditionsOperation in experiment
44% With edetate disodium; In tetrahydrofuran; for 0.5h; A mixture of benzyl acrylate (60.4 g, 372 mmol) and glycolaldehyde diethyl acetal (10.16 g, 74.5 mmol) in dry THF (70 mL) was stirred vigorously and Triton B (1.7 mL, 5 molpercent) was added. The RM became dark brown gradually over about 0.5 minutes during which an exotherm was noted. The reaction mixture was concentrated in vacuo and purified directly over silica-gel (330 g, Companion) eluting from 0-100percent EtOAc/cyclohexane to give the title compound as acolourless oil.Yield 9.7 g (44percent)1H NMR (400 MHz, CDCI3) 57.34-7.29 (m, 5H), 5.13 (s, 2H), 4.58 (t, J = 5.2Hz, 1H), 3.80, (t, J = 6.4 Hz, 2H), 3.67 (m, 2H), 3.54 (m, 2H), 3.46 (d, J = 5.2 Hz, 2H), 2.64 (t, J = 6.4 Hz, 2H), 1.20 (t, J = 7 Hz, 6H).
  • 5
  • [ 2495-35-4 ]
  • [ 20101-92-2 ]
  • (E)-benzyl 3-[2-(2-amino-2-oxoethyl)-5-chlorophenyl]acrylate [ No CAS ]
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