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2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid

Base Information Edit
  • Chemical Name:2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid
  • CAS No.:381226-91-1
  • Molecular Formula:C19H22N2O3
  • Molecular Weight:326.395
  • Hs Code.:
  • Mol file:381226-91-1.mol
2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid

Synonyms:2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid Edit
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Technology Process of 2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid

There total 14 articles about 2-[4-[2-[6-(methylamino)-2-pyridinyl]ethoxy]phenyl]cyclopropaneacetic acid 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 lithium hydroxide; In acetonitrile; at 55 ℃; for 2h;
DOI:10.1016/j.bmc.2007.03.020
Guidance literature:
Multi-step reaction with 3 steps
1: 89 percent / boron tribromide / CH2Cl2 / 18 h / 20 °C
2: triphenylphosphine; diisopropyl azodicarboxylate / tetrahydrofuran / 18 h / 20 °C
3: aq. LiOH / acetonitrile / 2 h / 55 °C
With lithium hydroxide; di-isopropyl azodicarboxylate; boron tribromide; triphenylphosphine; In tetrahydrofuran; dichloromethane; acetonitrile; 2: Mitsunobu reaction;
DOI:10.1016/j.bmc.2007.03.020
Guidance literature:
Multi-step reaction with 5 steps
1: 88 percent / sodium hydroxide / ethanol / 24 h / 20 °C
2: 82 percent / hydrochloric acid / 18 h / Heating
3: 89 percent / boron tribromide / CH2Cl2 / 18 h / 20 °C
4: triphenylphosphine; diisopropyl azodicarboxylate / tetrahydrofuran / 18 h / 20 °C
5: aq. LiOH / acetonitrile / 2 h / 55 °C
With hydrogenchloride; lithium hydroxide; sodium hydroxide; di-isopropyl azodicarboxylate; boron tribromide; triphenylphosphine; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile; 4: Mitsunobu reaction;
DOI:10.1016/j.bmc.2007.03.020
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