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3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose

Base Information
  • Chemical Name:3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose
  • CAS No.:75975-13-2
  • Molecular Formula:C30H31Br3O6
  • Molecular Weight:727.285
  • Hs Code.:
3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose

Synonyms:3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose

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Chemical Property of 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose
Chemical Property:
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Technology Process of 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose

There total 3 articles about 3-O-allyl-2,4,6-tri-O-(p-bromobenzyl)-D-mannopyranose 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:
Guidance literature:
With hydrogenchloride; In 1,4-dioxane; water; acetic acid; for 5h; Heating;
DOI:10.1021/jo00317a030
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / NaH / tetrahydrofuran / 1 h / Heating
2: 72 percent / KOH / toluene / Heating
3: concentrated HCl / acetic acid; dioxane; H2O / 5 h / Heating
With hydrogenchloride; potassium hydroxide; sodium hydride; In tetrahydrofuran; 1,4-dioxane; water; acetic acid; toluene;
DOI:10.1021/jo00317a030
Guidance literature:
Multi-step reaction with 2 steps
1: 72 percent / KOH / toluene / Heating
2: concentrated HCl / acetic acid; dioxane; H2O / 5 h / Heating
With hydrogenchloride; potassium hydroxide; In 1,4-dioxane; water; acetic acid; toluene;
DOI:10.1021/jo00317a030
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