C₂₃H₃₄O₅

Base Information

Chemical Name:C₂₃H₃₄O₅
CAS No.:74058-41-6
Molecular Formula:C₂₃H₃₄O₅
Molecular Weight:390.52
Hs Code.:

C<sub>23</sub>H<sub>34</sub>O<sub>5</sub>

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Suppliers and Price of C₂₃H₃₄O₅

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₃H₃₄O₅

Chemical Property:

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Technology Process of C₂₃H₃₄O₅

There total 12 articles about C₂₃H₃₄O₅ 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: 92.0%

: 74030-15-2
C₂₃H₃₂O₃

: 74058-41-6,74957-85-0
C₂₃H₃₄O₅

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol; for 22h; Ambient temperature;

Reference yield:

: 74030-12-9
5-methyl-2-(2-propenyl)-2-cyclohexen-1-one

: 74058-41-6,74957-85-0
C₂₃H₃₄O₅

Guidance literature:: Multi-step reaction with 5 steps

1: 29 percent / BF₃*Et₂O / CH₂Cl₂ / 240 h / Ambient temperature

2: 79 percent / p-toluenesulfonic acid / benzene / 4 h / Heating

3: 1.) BH₃, 2-methyl-2-butene, 2.) 3N NaOH, 30percent H₂O₂ / 1.) THF, 0 deg C, 2 h, 2.) THF, H₂O, 0-10 deg C

4: 83 percent / 50percent NaH / n-Bu₄N⁽¹⁺⁾*I^(1-) / hexamethylphosphoric acid triamide / 24 h / Ambient temperature

5: 92 percent / OsO₄, N-methylmorpholine-N-oxide / acetone; H₂O; 2-methyl-propan-2-ol / 22 h / Ambient temperature

With sodium hydroxide; osmium(VIII) oxide; 2-methyl-but-2-ene; boron trifluoride diethyl etherate; borane; dihydrogen peroxide; sodium hydride; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; tetra-(n-butyl)ammonium iodide; In N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; water; acetone; tert-butyl alcohol; benzene;

Reference yield:

: 100-39-0
benzyl bromide

: 74058-41-6,74957-85-0
C₂₃H₃₄O₅

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / 50percent NaH / n-Bu₄N⁽¹⁺⁾*I^(1-) / hexamethylphosphoric acid triamide / 24 h / Ambient temperature

2: 92 percent / OsO₄, N-methylmorpholine-N-oxide / acetone; H₂O; 2-methyl-propan-2-ol / 22 h / Ambient temperature

With osmium(VIII) oxide; sodium hydride; 4-methylmorpholine N-oxide; tetra-(n-butyl)ammonium iodide; In N,N,N,N,N,N-hexamethylphosphoric triamide; water; acetone; tert-butyl alcohol;