C₆₀H₆₆FN₆O₁₈P

Base Information

Chemical Name:C₆₀H₆₆FN₆O₁₈P
CAS No.:1055029-95-2
Molecular Formula:C₆₀H₆₆FN₆O₁₈P
Molecular Weight:1209.19
Hs Code.:

C<sub>60</sub>H<sub>66</sub>FN<sub>6</sub>O<sub>18</sub>P

Synonyms:

Suppliers and Price of C₆₀H₆₆FN₆O₁₈P

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 C₆₀H₆₆FN₆O₁₈P

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₆₀H₆₆FN₆O₁₈P

There total 10 articles about C₆₀H₆₆FN₆O₁₈P 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:

: 40615-36-9
4,4'-dimethoxytrityl chloride

: 1055029-95-2
C₆₀H₆₆FN₆O₁₈P

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / pyridine / CH₂Cl₂ / 1 h

2: 70 percent / diisopropylammonium tetrazolide / CH₂Cl₂ / 16 h

3: tetrazole / acetonitrile / 0.83 h

With pyridine; 1H-tetrazole; N,N-diisopropylamine tetrazolide; In dichloromethane; acetonitrile;
DOI:10.1021/jo9614607

Reference yield:

: 115012-52-7
1-(2-Fluorophenyl)-4-methoxy-1,2,5,6-tetrahydropyridine

: 1055029-95-2
C₆₀H₆₆FN₆O₁₈P

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / camphor-10-sulfonic acid / CH₂Cl₂ / 20 h

2: 76 percent / Et₃N*HF / tetrahydrofuran

3: 75 percent / pyridine / CH₂Cl₂ / 1 h

4: 70 percent / diisopropylammonium tetrazolide / CH₂Cl₂ / 16 h

5: tetrazole / acetonitrile / 0.83 h

With pyridine; 1H-tetrazole; camphor-10-sulfonic acid; N,N-diisopropylamine tetrazolide; triethylamine hydrofluoride; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jo9614607

Reference yield:

: 1-((2R,3R,3aS,9aR)-3-Allyl-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-4-hydroxy-1H-pyrimidin-2-one

: 1055029-95-2
C₆₀H₆₆FN₆O₁₈P

Guidance literature:: Multi-step reaction with 8 steps

1: 99.6 percent / N-methylmorpholine N-oxide, OsO₄ / acetone; H₂O / 1.5 h

2: NaIO₄ / dioxane; H₂O / 0.17 h

3: 100 percent / NaBH₄ / methanol / 0.33 h / 0 °C

4: 73 percent / camphor-10-sulfonic acid / CH₂Cl₂ / 20 h

5: 76 percent / Et₃N*HF / tetrahydrofuran

6: 75 percent / pyridine / CH₂Cl₂ / 1 h

7: 70 percent / diisopropylammonium tetrazolide / CH₂Cl₂ / 16 h

8: tetrazole / acetonitrile / 0.83 h

With pyridine; 1H-tetrazole; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; camphor-10-sulfonic acid; N,N-diisopropylamine tetrazolide; 4-methylmorpholine N-oxide; triethylamine hydrofluoride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; acetone; acetonitrile;
DOI:10.1021/jo9614607