C₁₉H₂₄F₃N₃O₅

Base Information

Chemical Name:C₁₉H₂₄F₃N₃O₅
CAS No.:1593758-44-1
Molecular Formula:C₁₉H₂₄F₃N₃O₅
Molecular Weight:431.412
Hs Code.:

C<sub>19</sub>H<sub>24</sub>F<sub>3</sub>N<sub>3</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C₁₉H₂₄F₃N₃O₅

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₁₉H₂₄F₃N₃O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₉H₂₄F₃N₃O₅

There total 5 articles about C₁₉H₂₄F₃N₃O₅ 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:

: 1593758-37-2
methyl (2R,3S)-2,3-dihydroxyoctanoate

: 1593758-44-1
C₁₉H₂₄F₃N₃O₅

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / ethyl acetate / 3 h / Inert atmosphere; Reflux

1.2: 0 - 20 °C / Inert atmosphere

2.1: sodium azide; water / acetone / 1.5 h / 20 °C

2.2: 48 h / 20 °C

With thionyl chloride; sodium azide; water; In ethyl acetate; acetone;
DOI:10.1021/ol500616v

Reference yield:

: 1593758-40-7
methyl (4R,5S)-5-pentyl-1,3,2-dioxathiolane-4-carboxylate 2,2-dioxide

: 1593758-44-1
C₁₉H₂₄F₃N₃O₅

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium azide; water / acetone / 1.5 h / 20 °C

1.2: 48 h / 20 °C

With sodium azide; water; In acetone;
DOI:10.1021/ol500616v

Reference yield:

: 66-25-1
hexanal

: 1593758-44-1
C₁₉H₂₄F₃N₃O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: dichloromethane / 17 h / 20 °C / Inert atmosphere

2.1: methanesulfonamide; AD-mix-α; water / tert-butyl alcohol / 96 h / 0 °C / Inert atmosphere

3.1: thionyl chloride / ethyl acetate / 3 h / Inert atmosphere; Reflux

3.2: 0 - 20 °C / Inert atmosphere

4.1: sodium azide; water / acetone / 1.5 h / 20 °C

4.2: 48 h / 20 °C

With thionyl chloride; sodium azide; methanesulfonamide; AD-mix-α; water; In dichloromethane; ethyl acetate; acetone; tert-butyl alcohol; 1.1: |Wittig Olefination / 2.1: |Sharpless Dihydroxylation;
DOI:10.1021/ol500616v