C₅₈H₈₆N₂O₁₆S

Base Information

Chemical Name:C₅₈H₈₆N₂O₁₆S
CAS No.:401521-45-7
Molecular Formula:C₅₈H₈₆N₂O₁₆S
Molecular Weight:1099.39
Hs Code.:

C<sub>58</sub>H<sub>86</sub>N<sub>2</sub>O<sub>16</sub>S

Synonyms:C₅₈H₈₆N₂O₁₆S

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Chemical Property of C₅₈H₈₆N₂O₁₆S

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Technology Process of C₅₈H₈₆N₂O₁₆S

There total 4 articles about C₅₈H₈₆N₂O₁₆S 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: 21.0%

: 401521-44-6
(10E)-10,11-didehydro-11-deoxy-6-O-methyl-erythromycin 2'-acetate 4''-(phenylmethyl carbonate) 12-[[[3-(pyridin-4-yl)propyl]thio]acetate]

: 401521-45-7
C₅₈H₈₆N₂O₁₆S

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; N,N-dimethyl-formamide; at 0 ℃; for 3h;
DOI:10.1016/j.bmc.2004.04.039

Reference yield:

: 2629-72-3
4-(3-Hydroxypropyl)pyridine

: 401521-45-7
C₅₈H₈₆N₂O₁₆S

Guidance literature:: Multi-step reaction with 5 steps

1.1: 65 percent / triphenylphosphine; diisopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C

2.1: NaBH₄ / ethanol / 20 °C

2.2: NaOEt / ethanol

3.1: NaOH / dioxane / 12 h / 20 °C

4.1: 413 mg / 4-dimethylaminopyridine; N,N'-dicyclohexylcarbodiimide / CH₂Cl₂ / 48 h / 20 °C

5.1: 21 percent / potassium tert-butylate / dimethylformamide; tetrahydrofuran / 3 h / 0 °C

With dmap; sodium hydroxide; sodium tetrahydroborate; di-isopropyl azodicarboxylate; potassium tert-butylate; dicyclohexyl-carbodiimide; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; 1.1: Mitsunobu reaction / 5.1: Michael addition;
DOI:10.1016/j.bmc.2004.04.039

Reference yield:

: 401521-43-5
[[3-(pyridin-4-yl)propyl]thio]acetic acid

: 401521-45-7
C₅₈H₈₆N₂O₁₆S

Guidance literature:: Multi-step reaction with 2 steps

1: 413 mg / 4-dimethylaminopyridine; N,N'-dicyclohexylcarbodiimide / CH₂Cl₂ / 48 h / 20 °C

2: 21 percent / potassium tert-butylate / dimethylformamide; tetrahydrofuran / 3 h / 0 °C

With dmap; potassium tert-butylate; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 2: Michael addition;
DOI:10.1016/j.bmc.2004.04.039