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[ CAS No. 16415-13-7 ] {[proInfo.proName]}

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Chemical Structure| 16415-13-7
Chemical Structure| 16415-13-7
Structure of 16415-13-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 16415-13-7 ]

CAS No. :16415-13-7 MDL No. :MFCD00054793
Formula : C22H48O3Si Boiling Point : -
Linear Structure Formula :- InChI Key :OYGYKEULCAINCL-UHFFFAOYSA-N
M.W : 388.70 Pubchem ID :85407
Synonyms :

Safety of [ 16415-13-7 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 16415-13-7 ]

* 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 [ 16415-13-7 ]

[ 16415-13-7 ] Synthesis Path-Downstream   1~11

  • 2
  • [ 998-30-1 ]
  • [ 629-73-2 ]
  • [ 16415-13-7 ]
YieldReaction ConditionsOperation in experiment
for 46h; Heating;
100 %Chromat. With hydridochlorotris(triphenylphosphine)ruthenium(II); tris(dibutylamino)(dioctylamino)phosphonium hexafluorophosphate at 95℃; for 2h;
76 %Spectr. With [Rh(OH)cod]2 and diethylaminopropyltrimethoxysilane immobilized on SiO2 In neat (no solvent) at 40℃; for 0.5h;
  • 3
  • [ 16415-13-7 ]
  • [ 36653-82-4 ]
YieldReaction ConditionsOperation in experiment
With disodium hydrogenphosphate; water; 3-chloro-benzenecarboperoxoic acid 1.) methanol, RT, 24 h; Yield given. Multistep reaction;
YieldReaction ConditionsOperation in experiment
Trichlorhexadecylsilan, Ethanol;
Trichlor-hexadecyl-silan, EtOH;
With particular preference, the alkoxysilanes set out below are prepared by the process of the invention: ... octyltriethoxysilane, cyclohexyltrimethoxysilane, cyclohexylmethyldimethoxysilane, hexadecyltrimethoxysilane, hexadecyltriethoxysilane.
  • 7
  • [ 16415-13-7 ]
  • C16H33Cl7O2Si3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: H2O 2: tetrachlorosilane / tetrahydrofuran; hexane / 20 °C
  • 8
  • [ 16415-13-7 ]
  • C16H33Cl9O3Si4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: H2O 2: tetrachlorosilane / tetrahydrofuran; hexane / 20 °C
  • 9
  • POM-7 [ No CAS ]
  • [ 66-40-0 ]
  • [ 16415-13-7 ]
  • [tetraethylammonium]3[PW11O39(Si(CH2)15CH3)2] [ No CAS ]
YieldReaction ConditionsOperation in experiment
With HCl In not given treatment of tungstate deriv. with silicate deriv. in presence of tetraethylammonium ions; elem. anal.;
  • 10
  • POM-7 [ No CAS ]
  • [ 10549-76-5 ]
  • [ 16415-13-7 ]
  • [Bu4N]3[PW11O39(Si(CH2)15CH3)2] [ No CAS ]
YieldReaction ConditionsOperation in experiment
With HCl In not given treatment of tungstate deriv. with silicate deriv. in presence of tetrabutylammonium ions; elem. anal.;
  • 11
  • [ 60-12-8 ]
  • [ 16415-13-7 ]
  • [ 1185275-68-6 ]
  • hexadecylsilicic acid bis(2-phenylethyl) ethyl ester [ No CAS ]
  • C64H102O5Si2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium methylate In methanol at 113 - 120℃; for 5h; Inert atmosphere; 3 Preparation Example 3
Preparation of a functional substance-releasing agent containing hexadecylsilicic acid tris (2-phenylethyl)ester[tris (2-phenylethyloxy)hexadecylsilane] In a 200 mL four-neck flask, under nitrogen flow, 50.56 g of hexadecyltriethoxysilane (0.13 mol), 44.43 g of 2-phenylethanol (0.36 mol), and 0.375 mL of 2.8% sodium methoxide in methanol were stirred for two hours at 113 to 120° C. with distilling off ethanol. After two hours, an inner pressure of the flask was gradually reduced to 8 kPa, and the mixture was stirred for additional three hours at 120° C. with distilling off ethanol. After three hours, the mixture was cooled and the reduced pressure was released. Then, the mixture was filtered to give 77.52 g of yellow oil containing hexadecylsilicic acid tris(2-phenylethyl)ester. The resultant oil was analyzed by GC. The result is shown in Table 3. From the result, contents of hexadecylsilicic acid tris(2-phenylethyl)ester of the compound (1) and hexadecylsilicic acid bis(2-phenylethyl)ethyl ester of the compound (2) were 69.9% and 19.9%, respectively.
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