C₂₃H₃₀FNO₂Si

Base Information

Chemical Name:C₂₃H₃₀FNO₂Si
CAS No.:1609683-20-6
Molecular Formula:C₂₃H₃₀FNO₂Si
Molecular Weight:399.581
Hs Code.:

C<sub>23</sub>H<sub>30</sub>FNO<sub>2</sub>Si

Synonyms:C₂₃H₃₀FNO₂Si

Suppliers and Price of C₂₃H₃₀FNO₂Si

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 C₂₃H₃₀FNO₂Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₃H₃₀FNO₂Si

There total 4 articles about C₂₃H₃₀FNO₂Si 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:

: 1609683-14-8
C₁₇H₂₃NO₂Si

: 352-13-6
4-flourophenylmagnesium bromide

: 1609683-20-6
C₂₃H₃₀FNO₂Si

Guidance literature:: C₁₇H₂₃NO₂Si; 4-flourophenylmagnesium bromide; In diethyl ether; at 0 - 20 ℃; for 2.08333h;

With zinc(II) tetrahydroborate; In tetrahydrofuran; methanol; diethyl ether; at -78 ℃; diastereoselective reaction;
DOI:10.1055/s-0033-1340251

Reference yield:

: 768-60-5
4-methoxyphenylacetylen

: 1609683-20-6
C₂₃H₃₀FNO₂Si

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran

2.1: (S)-hydroxynitrile lyase / tert-butyl methyl ether / 4 h / 0 °C / pH 5 / Enzymatic reaction

3.1: 1H-imidazole; dmap / dichloromethane / 0 - 20 °C

4.1: diethyl ether / 2.08 h / 0 - 20 °C

4.2: -78 °C

With 1H-imidazole; dmap; (S)-hydroxynitrile lyase; n-butyllithium; In tetrahydrofuran; diethyl ether; dichloromethane; tert-butyl methyl ether; 4.1: |Grignard Reaction;
DOI:10.1055/s-0033-1340251

Reference yield:

: 1609683-08-0
C₁₁H₉NO₂

: 1609683-20-6
C₂₃H₃₀FNO₂Si

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1H-imidazole; dmap / dichloromethane / 0 - 20 °C

2.1: diethyl ether / 2.08 h / 0 - 20 °C

2.2: -78 °C

With 1H-imidazole; dmap; In diethyl ether; dichloromethane; 2.1: |Grignard Reaction;
DOI:10.1055/s-0033-1340251