C₂₅H₃₉NO₃

Base Information

Chemical Name:C₂₅H₃₉NO₃
CAS No.:1408154-78-8
Molecular Formula:C₂₅H₃₉NO₃
Molecular Weight:401.59
Hs Code.:

C<sub>25</sub>H<sub>39</sub>NO<sub>3</sub>

Synonyms:C₂₅H₃₉NO₃

Suppliers and Price of C₂₅H₃₉NO₃

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 C₂₅H₃₉NO₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₅H₃₉NO₃

There total 10 articles about C₂₅H₃₉NO₃ 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: 91.0%

: 1408154-77-7
C₂₄H₃₇NO₃

: 74-88-4
methyl iodide

: 1408154-78-8
C₂₅H₃₉NO₃

Guidance literature:: With sodium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃;
DOI:10.1016/j.tetlet.2012.08.112

Reference yield:

: 1408154-79-9
C₁₄H₂₈O

: 1408154-78-8
C₂₅H₃₉NO₃

Guidance literature:: Multi-step reaction with 3 steps

1: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol / 20 °C

2: pivaloyl chloride; triethylamine; lithium chloride / tetrahydrofuran / -20 - 0 °C

3: sodium hexamethyldisilazane / tetrahydrofuran / -78 °C

With sodium chlorite; sodium dihydrogenphosphate; sodium hexamethyldisilazane; pivaloyl chloride; triethylamine; lithium chloride; In tetrahydrofuran; water; tert-butyl alcohol;
DOI:10.1016/j.tetlet.2012.08.112

Reference yield:

: C₂₃H₄₂O₄SSi

: 1408154-78-8
C₂₅H₃₉NO₃

Guidance literature:: Multi-step reaction with 9 steps

1: dilithium tetrachlorocuprate / diethyl ether / -78 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 °C

3: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C

5: diisobutylaluminium hydride / dichloromethane / -78 °C

6: 10 wt% Pd(OH)2 on carbon; triethylamine / benzene / 20 °C

7: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol / 20 °C

8: pivaloyl chloride; triethylamine; lithium chloride / tetrahydrofuran / -20 - 0 °C

9: sodium hexamethyldisilazane / tetrahydrofuran / -78 °C

With sodium chlorite; sodium dihydrogenphosphate; oxalyl dichloride; dilithium tetrachlorocuprate; 10 wt% Pd(OH)2 on carbon; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; pivaloyl chloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; lithium chloride; In tetrahydrofuran; diethyl ether; dichloromethane; water; tert-butyl alcohol; benzene; 1: |Grignard Reaction / 3: |Swern Oxidation / 4: |Wittig Olefination;
DOI:10.1016/j.tetlet.2012.08.112