9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

Base Information

Chemical Name:9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine
CAS No.:161545-38-6
Molecular Formula:C₄₁H₃₃N₅O₁₀
Molecular Weight:755.741
Hs Code.:

9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N<sup>6</sup>-benzoyladenine

Synonyms:9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

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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 9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

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Technology Process of 9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

There total 1 articles about 9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine 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: 79.0%

: 4005-49-6
N-benzoyladenine

: 1',2'-di-O-acetyl-3',5',6'-tri-O-benzoylglucofuranose

: 161545-38-6
9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

Guidance literature:: With tin(IV) chloride; In acetonitrile; Ambient temperature;
DOI:10.1135/cccc19941408

Reference yield: 83.0%

: 161545-38-6
9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

: 161545-39-7
9-(3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)adenine

Guidance literature:: With hydrazine hydrate; In pyridine; acetic acid; for 48h; Ambient temperature;
DOI:10.1135/cccc19941408

Reference yield:

: 161545-38-6
9-(2-O-acetyl-3,5,6-tri-O-benzoyl-β-D-glucofuranosyl)-N⁶-benzoyladenine

: 161545-40-0
9-(3,5,6-tri-O-benzoyl-2-O-methanesulfonyl-β-D-glucofuranosyl)adenine

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / hydrazine hydrate / acetic acid; pyridine / 48 h / Ambient temperature

2: 77 percent / pyridine / 5 h / Ambient temperature

With pyridine; hydrazine hydrate; In pyridine; acetic acid;
DOI:10.1135/cccc19941408