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C14H19F3NO14P3

Base Information
  • Chemical Name:C14H19F3NO14P3
  • CAS No.:1364927-49-0
  • Molecular Formula:C14H19F3NO14P3
  • Molecular Weight:575.22
  • Hs Code.:
C<sub>14</sub>H<sub>19</sub>F<sub>3</sub>NO<sub>14</sub>P<sub>3</sub>

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Chemical Property of C14H19F3NO14P3
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Technology Process of C14H19F3NO14P3

There total 10 articles about C14H19F3NO14P3 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
C14H16F3NO5; With trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate; at -15 - -10 ℃; Inert atmosphere;
With tributyl-amine; tri-n-butylamine pyrophosphate; In N,N-dimethyl-formamide; at -10 ℃; for 0.5h; Inert atmosphere;
DOI:10.1002/chem.201102066
Guidance literature:
Multi-step reaction with 5 steps
1.1: pyridine / 2.15 h / 20 °C / Inert atmosphere
2.1: palladium 10% on activated carbon; hydrogen; triethylamine / ethyl acetate / 1 h / 20 °C / Inert atmosphere
3.1: triethylamine / dichloromethane / 0.33 h / 10 °C / Inert atmosphere
4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere
5.1: trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate / -15 - -10 °C / Inert atmosphere
5.2: 0.5 h / -10 °C / Inert atmosphere
With pyridine; trimethyl phosphite; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1002/chem.201102066
Guidance literature:
Multi-step reaction with 8 steps
1.1: tributyl-amine; triphenyl-arsane; palladium diacetate / N,N-dimethyl-formamide / 15 h / 20 - 70 °C / Inert atmosphere
2.1: tetrabutyl ammonium fluoride / tetrahydrofuran; N,N-dimethyl-formamide / 2 h / 0 - 20 °C / Inert atmosphere
3.1: sodium triacetoxyborohydride; acetic acid / acetonitrile / 1 h / 0 °C / Inert atmosphere
4.1: pyridine / 2.15 h / 20 °C / Inert atmosphere
5.1: palladium 10% on activated carbon; hydrogen; triethylamine / ethyl acetate / 1 h / 20 °C / Inert atmosphere
6.1: triethylamine / dichloromethane / 0.33 h / 10 °C / Inert atmosphere
7.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere
8.1: trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate / -15 - -10 °C / Inert atmosphere
8.2: 0.5 h / -10 °C / Inert atmosphere
With pyridine; trimethyl phosphite; tributyl-amine; triphenyl-arsane; palladium 10% on activated carbon; sodium triacetoxyborohydride; tetrabutyl ammonium fluoride; hydrogen; palladium diacetate; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; acetic acid; triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; 1.1: Heck reaction;
DOI:10.1002/chem.201102066
upstream raw materials:

C17H36O3Si2

C15H14INO3

C24H43NO5Si2

C14H16F3NO5

Downstream raw materials:

C12H20NO13P3

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