C₄₃H₅₄O₈

Base Information

Chemical Name:C₄₃H₅₄O₈
CAS No.:1421916-96-2
Molecular Formula:C₄₃H₅₄O₈
Molecular Weight:698.897
Hs Code.:

C<sub>43</sub>H<sub>54</sub>O<sub>8</sub>

Synonyms:C₄₃H₅₄O₈

Suppliers and Price of C₄₃H₅₄O₈

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 C₄₃H₅₄O₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₃H₅₄O₈

There total 12 articles about C₄₃H₅₄O₈ 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: 71.0%

: C₄₉H₆₈O₈Si

: 1421916-96-2
C₄₃H₅₄O₈

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; for 1h; Inert atmosphere;
DOI:10.1016/j.steroids.2012.10.021

Reference yield:

: C₄₂H₆₄O₇Si

: 1421916-96-2
C₄₃H₅₄O₈

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; magnesium dibromide etherate / dichloromethane / 2 h / 25 °C / Inert atmosphere

2: boron trifluoride diethyl etherate / dichloromethane / 1 h / Inert atmosphere

With boron trifluoride diethyl etherate; magnesium dibromide etherate; triethylamine; In dichloromethane;
DOI:10.1016/j.steroids.2012.10.021

Reference yield:

: 227178-66-7
3β-acetoxy-12β-hydroxy-5α-spirostan-14-ene

: 1421916-96-2
C₄₃H₅₄O₈

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine / 6 h / Inert atmosphere

2: triethylsilane; boron trifluoride diethyl etherate / dichloromethane / 19 h / 0 - 25 °C / Inert atmosphere

3: triphenylphosphine; 1H-imidazole; iodine / tetrahydrofuran / 2.5 h / 20 °C / Inert atmosphere

4: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 12 h / 25 °C / Inert atmosphere

5: hydroquinidein 1,4-phthalazinediyl diether; potassium carbonate; potassium hexacyanoferrate(III); potassium osmate(VI) / water; tert-butyl alcohol / 18 h / 0 °C / Inert atmosphere

6: 1H-imidazole; dmap / dichloromethane / 1 h / 25 °C / Inert atmosphere

7: triethylamine; magnesium dibromide etherate / dichloromethane / 2 h / 25 °C / Inert atmosphere

8: boron trifluoride diethyl etherate / dichloromethane / 1 h / Inert atmosphere

With pyridine; 1H-imidazole; triethylsilane; dmap; potassium osmate(VI); boron trifluoride diethyl etherate; iodine; potassium carbonate; magnesium dibromide etherate; 1,8-diazabicyclo[5.4.0]undec-7-ene; hydroquinidein 1,4-phthalazinediyl diether; triethylamine; triphenylphosphine; potassium hexacyanoferrate(III); In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/j.steroids.2012.10.021