C₁₈H₃₀FN₂O₆P

Base Information

Chemical Name:C₁₈H₃₀FN₂O₆P
CAS No.:1114393-83-7
Molecular Formula:C₁₈H₃₀FN₂O₆P
Molecular Weight:420.418
Hs Code.:

C<sub>18</sub>H<sub>30</sub>FN<sub>2</sub>O<sub>6</sub>P

Synonyms:

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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 C₁₈H₃₀FN₂O₆P

Chemical Property:

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Technology Process of C₁₈H₃₀FN₂O₆P

There total 5 articles about C₁₈H₃₀FN₂O₆P 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:

: 1114394-71-6
C₂₇H₄₆FN₂O₈P

: 1114393-83-7
C₁₈H₃₀FN₂O₆P

Guidance literature:: With trimethylsilyl bromide; In dichloromethane;
DOI:10.1016/j.bmcl.2008.11.072

Reference yield:

: 111-83-1
1-bromo-octane

: 1114393-83-7
C₁₈H₃₀FN₂O₆P

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate; sodium iodide / N,N-dimethyl-formamide / 60 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane

3: triethylamine / dichloromethane

4: trimethylsilyl bromide / dichloromethane

With trimethylsilyl bromide; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium iodide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2008.11.072

Reference yield:

: 1114394-21-6
C₂₃H₃₇FN₂O₅

: 1114393-83-7
C₁₈H₃₀FN₂O₆P

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane

2: trimethylsilyl bromide / dichloromethane

With trimethylsilyl bromide; triethylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2008.11.072