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Phosphinic acid, [(2R,3S)-4-hydroxy-2,3-dimethoxybutyl]phenyl-, ethyl ester

Base Information Edit
  • Chemical Name:Phosphinic acid, [(2R,3S)-4-hydroxy-2,3-dimethoxybutyl]phenyl-, ethyl ester
  • CAS No.:880359-10-4
  • Molecular Formula:C14H23O5P
  • Molecular Weight:302.307
  • Hs Code.:
  • Mol file:880359-10-4.mol
Phosphinic acid, [(2R,3S)-4-hydroxy-2,3-dimethoxybutyl]phenyl-, ethyl
ester

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Phosphinic acid, [(2R,3S)-4-hydroxy-2,3-dimethoxybutyl]phenyl-, ethyl ester Edit
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Technology Process of Phosphinic acid, [(2R,3S)-4-hydroxy-2,3-dimethoxybutyl]phenyl-, ethyl ester

There total 5 articles about Phosphinic acid, [(2R,3S)-4-hydroxy-2,3-dimethoxybutyl]phenyl-, ethyl ester 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 hydrogen; palladium dihydroxide; In ethanol; at 20 ℃; for 6h;
DOI:10.3987/COM-05-S(K)15
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / 3 h / 150 °C
2: 92 percent / H2 / Pd(OH)2/C / ethanol / 6 h / 20 °C
With hydrogen; palladium dihydroxide; In ethanol; 1: Michaelis-Arbuzov reaction;
DOI:10.3987/COM-05-S(K)15
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium hydride / 1,2-dimethoxy-ethane / 1 h / 20 °C
1.2: 80 percent / 1,2-dimethoxy-ethane / 8 h / 20 °C
2.1: 55 percent / carbon tetrabromide; triphenylphosphine / CHCl3 / 6 h / 0 - 5 °C
3.1: 93 percent / 3 h / 150 °C
4.1: 92 percent / H2 / Pd(OH)2/C / ethanol / 6 h / 20 °C
With carbon tetrabromide; hydrogen; sodium hydride; triphenylphosphine; palladium dihydroxide; In 1,2-dimethoxyethane; ethanol; chloroform; 3.1: Michaelis-Arbuzov reaction;
DOI:10.3987/COM-05-S(K)15
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