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Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid

Base Information
  • Chemical Name:Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid
  • CAS No.:55734-52-6
  • Molecular Formula:C19H16Br2O5
  • Molecular Weight:484.141
  • Hs Code.:
Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid

Synonyms:Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid

Suppliers and Price of Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid
Chemical Property:
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Technology Process of Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid

There total 4 articles about Di-O-benzoyl-2-brom-2-deoxy-D-arabinosylbromid 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:
Multi-step reaction with 3 steps
1: pyridine / dichloromethane / 2.78 h / -30 - -4 °C / Inert atmosphere
2: lithium bromide / 1-methyl-pyrrolidin-2-one / 20 h / 20 °C / Inert atmosphere
3: hydrogen bromide; acetic acid / dichloromethane / 23 h / 20 °C / Inert atmosphere
With pyridine; hydrogen bromide; acetic acid; lithium bromide; In 1-methyl-pyrrolidin-2-one; dichloromethane;
DOI:10.1021/op800182x
Guidance literature:
With hydrogen bromide; acetic acid; In dichloromethane; at 20 ℃; for 23h; Inert atmosphere;
DOI:10.1021/op800182x
Guidance literature:
Multi-step reaction with 2 steps
1: lithium bromide / 1-methyl-pyrrolidin-2-one / 20 h / 20 °C / Inert atmosphere
2: hydrogen bromide; acetic acid / dichloromethane / 23 h / 20 °C / Inert atmosphere
With hydrogen bromide; acetic acid; lithium bromide; In 1-methyl-pyrrolidin-2-one; dichloromethane;
DOI:10.1021/op800182x
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