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(2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide

Base Information Edit
  • Chemical Name:(2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide
  • CAS No.:1259430-48-2
  • Molecular Formula:C14H21NO3
  • Molecular Weight:251.326
  • Hs Code.:
  • Mol file:1259430-48-2.mol
(2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide

Synonyms:(2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide Edit
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Technology Process of (2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide

There total 3 articles about (2SR)-N-(benzyloxy)-5-hydroxy-2,4-dimethylpentanamide 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 methanol; sodium tetrahydroborate; at 0 - 20 ℃; for 18.5h; Inert atmosphere;
DOI:10.1002/ejoc.201101222
Guidance literature:
Multi-step reaction with 3 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.17 h / 20 °C / Inert atmosphere
1.2: 0.5 h / Inert atmosphere
2.1: dichloromethane / 72 h / 20 °C / Inert atmosphere
3.1: methanol; sodium tetrahydroborate / 18.5 h / 0 - 20 °C / Inert atmosphere
With methanol; sodium tetrahydroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane;
DOI:10.1002/ejoc.201101222
Guidance literature:
Multi-step reaction with 2 steps
1: dichloromethane / 72 h / 20 °C / Inert atmosphere
2: methanol; sodium tetrahydroborate / 18.5 h / 0 - 20 °C / Inert atmosphere
With methanol; sodium tetrahydroborate; In dichloromethane;
DOI:10.1002/ejoc.201101222
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