C₁₉H₂₇NO₆

Base Information

Chemical Name:C₁₉H₂₇NO₆
CAS No.:1469300-19-3
Molecular Formula:C₁₉H₂₇NO₆
Molecular Weight:365.426
Hs Code.:

C<sub>19</sub>H<sub>27</sub>NO<sub>6</sub>

Synonyms:C₁₉H₂₇NO₆

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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 C₁₉H₂₇NO₆

Chemical Property:

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Technology Process of C₁₉H₂₇NO₆

There total 4 articles about C₁₉H₂₇NO₆ 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: 80.0%

: 24424-99-5
di-tert-butyl dicarbonate

: methyl 2,5-anhydro-6-azido-3,6-dideoxy-d-ribo-hexonate

: 1469300-19-3
C₁₉H₂₇NO₆

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethyl acetate; for 6h; under 760.051 Torr;
DOI:10.1002/anie.201304239

Reference yield:

: C₁₃H₁₇N₃O₃

: 1469300-19-3
C₁₉H₂₇NO₆

Guidance literature:: Multi-step reaction with 3 steps

1: boron trifluoride diethyl etherate / acetonitrile / 0.17 h / 0 °C / Inert atmosphere

2: acetyl chloride / 4.5 h / 0 - 50 °C / Inert atmosphere

3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 6 h / 760.05 Torr

With palladium 10% on activated carbon; boron trifluoride diethyl etherate; hydrogen; acetyl chloride; In ethyl acetate; acetonitrile;
DOI:10.1002/anie.201304239

Reference yield:

: 1469300-25-1
C₁₃H₁₄N₄O₂

: 1469300-19-3
C₁₉H₂₇NO₆

Guidance literature:: Multi-step reaction with 2 steps

1: acetyl chloride / 4.5 h / 0 - 50 °C / Inert atmosphere

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 6 h / 760.05 Torr

With palladium 10% on activated carbon; hydrogen; acetyl chloride; In ethyl acetate;
DOI:10.1002/anie.201304239