C₃₀H₄₂O₇

Base Information

Chemical Name:C₃₀H₄₂O₇
CAS No.:350583-40-3
Molecular Formula:C₃₀H₄₂O₇
Molecular Weight:514.659
Hs Code.:

C<sub>30</sub>H<sub>42</sub>O<sub>7</sub>

Synonyms:C₃₀H₄₂O₇

Suppliers and Price of C₃₀H₄₂O₇

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 C₃₀H₄₂O₇

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₄₂O₇

There total 11 articles about C₃₀H₄₂O₇ 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%

: 350583-39-0
C₃₆H₅₆O₇Si

: 350583-40-3
C₃₀H₄₂O₇

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 0.166667h;
DOI:10.1002/1099-0690(200105)2001:9<1761::AID-EJOC1761>3.0.CO;2-O

Reference yield:

: C₃₉H₄₄O₇

: 350583-40-3
C₃₀H₄₂O₇

Guidance literature:: Multi-step reaction with 11 steps

1: 76 percent / aq. NaOH / tetrahydrofuran / 48 h / Heating

2: 93 percent / pyridine / 96 h / 20 °C

3: PBu₃; NEt₃; HCOOH / Pd(dba)2 / tetrahydrofuran / Heating

4: 67 percent / OsO₄; NMMO / tetrahydrofuran; H₂O; 2-methyl-propan-2-ol / 144 h / 20 °C

5: 61 percent / DIBALH / CH₂Cl₂; toluene / 0.5 h

6: 99 percent / sodium periodate / tetrahydrofuran; H₂O / 72 h / 20 °C

7: 92 percent / imidazole / dimethylformamide / 5 h / 20 °C

8: 88 percent / NaBH₄ / methanol / 0.33 h / 0 °C

9: 57 percent / n-butyllithium / tetrahydrofuran; hexane / 20 h / 20 °C

10: 48 percent / tert-butyl hydroperoxide; palladium(II) acetate / toluene / 72 h / 50 °C

11: 91 percent / tetrabutylammonium fluoride / tetrahydrofuran / 0.17 h / 20 °C

With 1H-imidazole; tert.-butylhydroperoxide; sodium hydroxide; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; n-butyllithium; formic acid; tributylphosphine; tetrabutyl ammonium fluoride; palladium diacetate; diisobutylaluminium hydride; 4-methylmorpholine N-oxide; triethylamine; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In tetrahydrofuran; pyridine; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; toluene; tert-butyl alcohol;
DOI:10.1002/1099-0690(200105)2001:9<1761::AID-EJOC1761>3.0.CO;2-O

Reference yield:

: 350583-27-6
1,2-benzylidene-9,10-isopropylidene-5α-acetyltaxicin-I

: 350583-40-3
C₃₀H₄₂O₇

Guidance literature:: Multi-step reaction with 9 steps

1: PBu₃; NEt₃; HCOOH / Pd(dba)2 / tetrahydrofuran / Heating

2: 67 percent / OsO₄; NMMO / tetrahydrofuran; H₂O; 2-methyl-propan-2-ol / 144 h / 20 °C

3: 61 percent / DIBALH / CH₂Cl₂; toluene / 0.5 h

4: 99 percent / sodium periodate / tetrahydrofuran; H₂O / 72 h / 20 °C

5: 92 percent / imidazole / dimethylformamide / 5 h / 20 °C

6: 88 percent / NaBH₄ / methanol / 0.33 h / 0 °C

7: 57 percent / n-butyllithium / tetrahydrofuran; hexane / 20 h / 20 °C

8: 48 percent / tert-butyl hydroperoxide; palladium(II) acetate / toluene / 72 h / 50 °C

9: 91 percent / tetrabutylammonium fluoride / tetrahydrofuran / 0.17 h / 20 °C

With 1H-imidazole; tert.-butylhydroperoxide; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; n-butyllithium; formic acid; tributylphosphine; tetrabutyl ammonium fluoride; palladium diacetate; diisobutylaluminium hydride; 4-methylmorpholine N-oxide; triethylamine; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In tetrahydrofuran; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; toluene; tert-butyl alcohol;
DOI:10.1002/1099-0690(200105)2001:9<1761::AID-EJOC1761>3.0.CO;2-O