C₁₇H₂₆O₇

Base Information

Chemical Name:C₁₇H₂₆O₇
CAS No.:1608472-91-8
Molecular Formula:C₁₇H₂₆O₇
Molecular Weight:342.389
Hs Code.:

C<sub>17</sub>H<sub>26</sub>O<sub>7</sub>

Synonyms:

Suppliers and Price of C₁₇H₂₆O₇

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 C₁₇H₂₆O₇

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₇H₂₆O₇

There total 8 articles about C₁₇H₂₆O₇ 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:

: 1608473-19-3
(2R,3S,4S)-4-[(4-methoxybenzyl)oxy]-2,3-bis(methoxymethoxy)pentan-1-ol

: 1608472-91-8
C₁₇H₂₆O₇

Guidance literature:: (2R,3S,4S)-4-[(4-methoxybenzyl)oxy]-2,3-bis(methoxymethoxy)pentan-1-ol; With oxalyl dichloride; In dichloromethane; dimethyl sulfoxide; at -78 ℃; for 1.5h; Inert atmosphere;

With triethylamine; In dichloromethane; dimethyl sulfoxide; at -78 - 0 ℃; for 1h; Inert atmosphere;
DOI:10.1002/ejoc.201301215

Reference yield:

: 1608472-94-1
(2R,3R,4S)-4-[(4-methoxybenzyl)oxy]pentane-1,2,3-triol

: 1608472-91-8
C₁₇H₂₆O₇

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1H-imidazole / dichloromethane / 0.25 h / 0 °C / Inert atmosphere

1.2: 1 h / 0 °C / Inert atmosphere

2.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

4.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / 1.5 h / -78 °C / Inert atmosphere

4.2: 1 h / -78 - 0 °C / Inert atmosphere

With 1H-imidazole; dmap; oxalyl dichloride; tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1002/ejoc.201301215

Reference yield:

: (-)-(2E)-(4S)-ethyl 4-(p-methoxybenzyl)oxy-2-pentenoate

: 1608472-91-8
C₁₇H₂₆O₇

Guidance literature:: Multi-step reaction with 7 steps

1.1: diisobutylaluminium hydride / dichloromethane / 1 h / 0 °C / Inert atmosphere

2.1: titanium(IV) isopropylate; L-(+)-diisopropyl tartrate / dichloromethane / 0.5 h / -20 °C / Inert atmosphere; Molecular sieve

2.2: 8 h / Inert atmosphere

3.1: sodium hydroxide / water; tert-butyl alcohol / 15 h / 70 °C / Inert atmosphere

4.1: 1H-imidazole / dichloromethane / 0.25 h / 0 °C / Inert atmosphere

4.2: 1 h / 0 °C / Inert atmosphere

5.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

7.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / 1.5 h / -78 °C / Inert atmosphere

7.2: 1 h / -78 - 0 °C / Inert atmosphere

With 1H-imidazole; titanium(IV) isopropylate; dmap; oxalyl dichloride; L-(+)-diisopropyl tartrate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; tert-butyl alcohol; 2.1: |Sharpless Asymmetric Epoxidation / 2.2: |Sharpless Allylic Amination;
DOI:10.1002/ejoc.201301215