C₆₃H₇₁N₃O₉Si

Base Information

Chemical Name:C₆₃H₇₁N₃O₉Si
CAS No.:1621925-76-5
Molecular Formula:C₆₃H₇₁N₃O₉Si
Molecular Weight:1042.36
Hs Code.:

C<sub>63</sub>H<sub>71</sub>N<sub>3</sub>O<sub>9</sub>Si

Synonyms:C₆₃H₇₁N₃O₉Si

Suppliers and Price of C₆₃H₇₁N₃O₉Si

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 C₆₃H₇₁N₃O₉Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₆₃H₇₁N₃O₉Si

There total 22 articles about C₆₃H₇₁N₃O₉Si 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%

: 1242104-16-0
(2S,3aR,5R,6S,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)-5-hydroxyoctahydro-1H-indol-6-yl acetate

: 1621925-76-5
C₆₃H₇₁N₃O₉Si

Guidance literature:: With tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide; In dichloromethane; for 0.333333h; Inert atmosphere;
DOI:10.1002/chem.201400046

Reference yield:

: 1621925-46-9
C₃₇H₆₀N₂O₅Si₃

: 1621925-76-5
C₆₃H₇₁N₃O₉Si

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; fluorosilicic acid / water; acetonitrile / 12.5 h / 20 - 65 °C

2: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C / Inert atmosphere

3: 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate / dichloromethane / 0.33 h / Inert atmosphere

With fluorosilicic acid; tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; water; acetonitrile;
DOI:10.1002/chem.201400046

Reference yield:

: 162919-37-1
(S)-3-[4-(benzyloxy)phenyl]-2-hydroxypropanoic acid

: 1621925-76-5
C₆₃H₇₁N₃O₉Si

Guidance literature:: Multi-step reaction with 7 steps

1.1: dichloromethane; methanol; diethyl ether / 0.25 h / 0 - 20 °C / Inert atmosphere

2.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C / Inert atmosphere

2.2: 1.5 h / 20 °C / Inert atmosphere

3.1: methanol; lithium hydroxide monohydrate / tetrahydrofuran; water / 3 h / 20 °C

4.1: triethylamine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C / Inert atmosphere

5.1: methanol; lithium hydroxide monohydrate / tetrahydrofuran; water / 0.5 h / 20 °C

6.1: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C / Inert atmosphere

7.1: 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate / dichloromethane / 0.33 h / Inert atmosphere

With methanol; dmap; tetrapropylammonium perruthennate; lithium hydroxide monohydrate; sodium hydride; benzotriazol-1-ol; 4-methylmorpholine N-oxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water;
DOI:10.1002/chem.201400046