C₂₉H₄₁NO₆Si

Base Information

Chemical Name:C₂₉H₄₁NO₆Si
CAS No.:1265173-09-8
Molecular Formula:C₂₉H₄₁NO₆Si
Molecular Weight:527.733
Hs Code.:

C<sub>29</sub>H<sub>41</sub>NO<sub>6</sub>Si

Synonyms:C₂₉H₄₁NO₆Si

Suppliers and Price of C₂₉H₄₁NO₆Si

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 C₂₉H₄₁NO₆Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₉H₄₁NO₆Si

There total 16 articles about C₂₉H₄₁NO₆Si 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:

: C₂₁H₃₅NO₄Si

: 501-53-1,94274-21-2
benzyl chloroformate

: 1265173-09-8
C₂₉H₄₁NO₆Si

Guidance literature:: With potassium carbonate; In tetrahydrofuran; water; at 0 ℃; for 3h;
DOI:10.1002/asia.201000602

Reference yield:

: 1265173-20-3
C₂₂H₂₈O₇S

: 1265173-09-8
C₂₉H₄₁NO₆Si

Guidance literature:: Multi-step reaction with 11 steps

1.1: acetic anhydride; dimethyl sulfoxide / 2 h / 50 °C

2.1: toluene / 4 h / -40 °C

3.1: magnesium / methanol / 2 h / 20 °C

4.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / 4 h / 20 °C

5.1: sodium hydride / tetrahydrofuran; hexane; mineral oil / 0.17 h / 0 °C

5.2: 0 - 20 °C

6.1: pyridine / dichloromethane / 2 h / 0 °C

7.1: diisobutylaluminium hydride / toluene / 0.5 h / -78 °C

8.1: dichloromethane / 1 h / 0 °C

9.1: sodium carbonate / tert-butylbenzene / 24 h / 170 °C

10.1: diisobutylaluminium hydride / toluene / 1 h / -78 °C

11.1: potassium carbonate / tetrahydrofuran; water / 3 h / 0 °C

With pyridine; sulfur trioxide pyridine complex; acetic anhydride; sodium hydride; diisobutylaluminium hydride; sodium carbonate; potassium carbonate; magnesium; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; methanol; tert-butylbenzene; hexane; dichloromethane; water; toluene; mineral oil; 4.1: Swern oxidation / 5.2: Horner-Wadsworth-Emmons olefination / 9.1: Overman rearrangement;
DOI:10.1002/asia.201000602

Reference yield:

: 1265173-03-2
C₂₂H₂₆O₇S

: 1265173-09-8
C₂₉H₄₁NO₆Si

Guidance literature:: Multi-step reaction with 10 steps

1.1: toluene / 4 h / -40 °C

2.1: magnesium / methanol / 2 h / 20 °C

3.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / 4 h / 20 °C

4.1: sodium hydride / tetrahydrofuran; hexane; mineral oil / 0.17 h / 0 °C

4.2: 0 - 20 °C

5.1: pyridine / dichloromethane / 2 h / 0 °C

6.1: diisobutylaluminium hydride / toluene / 0.5 h / -78 °C

7.1: dichloromethane / 1 h / 0 °C

8.1: sodium carbonate / tert-butylbenzene / 24 h / 170 °C

9.1: diisobutylaluminium hydride / toluene / 1 h / -78 °C

10.1: potassium carbonate / tetrahydrofuran; water / 3 h / 0 °C

With pyridine; sulfur trioxide pyridine complex; sodium hydride; diisobutylaluminium hydride; sodium carbonate; potassium carbonate; magnesium; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; methanol; tert-butylbenzene; hexane; dichloromethane; water; toluene; mineral oil; 3.1: Swern oxidation / 4.2: Horner-Wadsworth-Emmons olefination / 8.1: Overman rearrangement;
DOI:10.1002/asia.201000602