C₁₇H₂₂O₅

Base Information

Chemical Name:C₁₇H₂₂O₅
CAS No.:1592771-58-8
Molecular Formula:C₁₇H₂₂O₅
Molecular Weight:306.359
Hs Code.:

C<sub>17</sub>H<sub>22</sub>O<sub>5</sub>

Synonyms:C₁₇H₂₂O₅

Suppliers and Price of C₁₇H₂₂O₅

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 C₁₇H₂₂O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₇H₂₂O₅

There total 9 articles about C₁₇H₂₂O₅ 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: 88.0%

: 1592771-55-5
C₁₇H₂₄O₅

: 1592771-58-8
C₁₇H₂₂O₅

Guidance literature:: With Dess-Martin periodane; In dichloromethane; at 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.1021/ol500788c

Reference yield:

: methyl 3-O-benzyl-5-O-(p-toluenesulfonyl)-2-deoxy-D-ribofuranoside

: 1592771-58-8
C₁₇H₂₂O₅

Guidance literature:: Multi-step reaction with 6 steps

1: lithium triethylborohydride / tetrahydrofuran / 6.25 h / 20 - 45 °C / Inert atmosphere

2: boron trifluoride diethyl etherate / dichloromethane / 0.67 h / 0 - 20 °C / Inert atmosphere

3: 4-methyl-morpholine / dichloromethane / 2 h / 20 °C / Inert atmosphere

4: methyl iodide; sodium hydrogencarbonate / acetonitrile; water / 24 h / 20 °C

5: samarium diiodide / acetonitrile; methanol / 1 h / -20 °C / Inert atmosphere

6: Dess-Martin periodane / dichloromethane / 1.5 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; samarium diiodide; boron trifluoride diethyl etherate; lithium triethylborohydride; sodium hydrogencarbonate; Dess-Martin periodane; methyl iodide; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile; 6: |Dess-Martin Oxidation;
DOI:10.1021/ol500788c

Reference yield:

: methyl 3-O-benzyl-2,5-dideoxy-D-erythropentofuranoside

: 1592771-58-8
C₁₇H₂₂O₅

Guidance literature:: Multi-step reaction with 5 steps

1: boron trifluoride diethyl etherate / dichloromethane / 0.67 h / 0 - 20 °C / Inert atmosphere

2: 4-methyl-morpholine / dichloromethane / 2 h / 20 °C / Inert atmosphere

3: methyl iodide; sodium hydrogencarbonate / acetonitrile; water / 24 h / 20 °C

4: samarium diiodide / acetonitrile; methanol / 1 h / -20 °C / Inert atmosphere

5: Dess-Martin periodane / dichloromethane / 1.5 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; samarium diiodide; boron trifluoride diethyl etherate; sodium hydrogencarbonate; Dess-Martin periodane; methyl iodide; In methanol; dichloromethane; water; acetonitrile; 5: |Dess-Martin Oxidation;
DOI:10.1021/ol500788c