C₃₁H₅₂O₈

Base Information

Chemical Name:C₃₁H₅₂O₈
CAS No.:1422550-02-4
Molecular Formula:C₃₁H₅₂O₈
Molecular Weight:552.749
Hs Code.:

C<sub>31</sub>H<sub>52</sub>O<sub>8</sub>

Synonyms:

Suppliers and Price of C₃₁H₅₂O₈

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 C₃₁H₅₂O₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₁H₅₂O₈

There total 10 articles about C₃₁H₅₂O₈ 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:

: C₃₁H₅₄O₇

: 1422550-02-4
C₃₁H₅₂O₈

Guidance literature:: With Jones reagent; In water; acetone; at -10 ℃;
DOI:10.1016/j.bmcl.2012.10.083

Reference yield:

: 1422530-87-7
C₁₇H₂₈O

: 1422550-02-4
C₃₁H₅₂O₈

Guidance literature:: Multi-step reaction with 8 steps

1: toluene-4-sulfonic acid / toluene / Reflux

2: Schwartz's reagent; methylmagnesium chloride; copper(l) iodide / tetrahydrofuran / -20 °C

3: pyridinium p-toluenesulfonate / dichloromethane

4: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran

5: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C

6: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol

7: acetic acid / tetrahydrofuran / 20 °C

8: Jones reagent / water; acetone / -10 °C

With sodium chlorite; sodium dihydrogenphosphate; copper(l) iodide; Jones reagent; Schwartz's reagent; oxalyl dichloride; tetrabutyl ammonium fluoride; methylmagnesium chloride; pyridinium p-toluenesulfonate; toluene-4-sulfonic acid; acetic acid; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; water; acetone; toluene; tert-butyl alcohol; 5: |Swern Oxidation;
DOI:10.1016/j.bmcl.2012.10.083

Reference yield:

: 1422531-83-6
C₁₉H₃₂O₂

: 1422550-02-4
C₃₁H₅₂O₈

Guidance literature:: Multi-step reaction with 7 steps

1: Schwartz's reagent; methylmagnesium chloride; copper(l) iodide / tetrahydrofuran / -20 °C

2: pyridinium p-toluenesulfonate / dichloromethane

3: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran

4: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C

5: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol

6: acetic acid / tetrahydrofuran / 20 °C

7: Jones reagent / water; acetone / -10 °C

With sodium chlorite; sodium dihydrogenphosphate; copper(l) iodide; Jones reagent; Schwartz's reagent; oxalyl dichloride; tetrabutyl ammonium fluoride; methylmagnesium chloride; pyridinium p-toluenesulfonate; acetic acid; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol; 4: |Swern Oxidation;
DOI:10.1016/j.bmcl.2012.10.083