C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

Base Information

Chemical Name:C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)
CAS No.:1548723-01-8
Molecular Formula:CF₃O₃S*C₂₃H₁₇F₁₇N₃O₅
Molecular Weight:887.448
Hs Code.:

C<sub>23</sub>H<sub>17</sub>F<sub>17</sub>N<sub>3</sub>O<sub>5</sub><sup>(1+)</sup>*CF<sub>3</sub>O<sub>3</sub>S<sup>(1-)</sup>

Synonyms:C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

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Technology Process of C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

There total 5 articles about C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-) 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:

Reference yield: 96.0%

: 1548722-99-1
C₂₂H₁₄F₁₇N₃O₅

: 333-27-7
methyl trifluoromethanesulfonate

: 1548723-01-8
C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

Guidance literature:: In diethyl ether; at 0 ℃; for 4h; Inert atmosphere;
DOI:10.1021/ol500023y

Reference yield:

: 908833-73-8
4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl methanesulfonate

: 1548723-01-8
C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 70 °C / Inert atmosphere

2: sodium tetrahydroborate / methanol / 0 - 25 °C / Inert atmosphere

3: acetonitrile / 16 h / 25 °C / Inert atmosphere

4: diethyl ether / 4 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; potassium carbonate; In methanol; diethyl ether; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/ol500023y

Reference yield:

: 1548722-86-6
C₁₈H₁₀F₁₇NO₄

: 1548723-01-8
C₂₃H₁₇F₁₇N₃O₅⁽¹⁺⁾*CF₃O₃S^(1-)

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate / methanol / 0 - 25 °C / Inert atmosphere

2: acetonitrile / 16 h / 25 °C / Inert atmosphere

3: diethyl ether / 4 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; In methanol; diethyl ether; acetonitrile;
DOI:10.1021/ol500023y