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1(2H)-Pyrazinecarboxylic acid, 3,4-dihydro-3-oxo-2-(phenylmethyl)-4-[3-[1-(triphenylmethyl)-1H-imidaz ol-4-yl]-2-propenyl]-, phenylmethyl ester, (2S)-

Base Information Edit
  • Chemical Name:1(2H)-Pyrazinecarboxylic acid, 3,4-dihydro-3-oxo-2-(phenylmethyl)-4-[3-[1-(triphenylmethyl)-1H-imidaz ol-4-yl]-2-propenyl]-, phenylmethyl ester, (2S)-
  • CAS No.:500782-79-6
  • Molecular Formula:C44H38N4O3
  • Molecular Weight:670.811
  • Hs Code.:
  • Mol file:500782-79-6.mol
1(2H)-Pyrazinecarboxylic acid,
3,4-dihydro-3-oxo-2-(phenylmethyl)-4-[3-[1-(triphenylmethyl)-1H-imidaz
ol-4-yl]-2-propenyl]-, phenylmethyl ester, (2S)-

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1(2H)-Pyrazinecarboxylic acid, 3,4-dihydro-3-oxo-2-(phenylmethyl)-4-[3-[1-(triphenylmethyl)-1H-imidaz ol-4-yl]-2-propenyl]-, phenylmethyl ester, (2S)- Edit
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Technology Process of 1(2H)-Pyrazinecarboxylic acid, 3,4-dihydro-3-oxo-2-(phenylmethyl)-4-[3-[1-(triphenylmethyl)-1H-imidaz ol-4-yl]-2-propenyl]-, phenylmethyl ester, (2S)-

There total 7 articles about 1(2H)-Pyrazinecarboxylic acid, 3,4-dihydro-3-oxo-2-(phenylmethyl)-4-[3-[1-(triphenylmethyl)-1H-imidaz ol-4-yl]-2-propenyl]-, phenylmethyl ester, (2S)- 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 sodium hydride; In tetrahydrofuran; at 60 ℃; for 2h;
DOI:10.1039/b517572k
Guidance literature:
Multi-step reaction with 3 steps
1: 75 percent / LiAlH4 / tetrahydrofuran
2: 75 percent / SOCl2 / tetrahydrofuran / 1 h
3: 21 percent / NaH / tetrahydrofuran / 2 h / 60 °C
With lithium aluminium tetrahydride; thionyl chloride; sodium hydride; In tetrahydrofuran;
DOI:10.1039/b517572k
Guidance literature:
Multi-step reaction with 3 steps
1: 86 percent / EDCI; DIEA / CH2Cl2 / 5 h / 20 °C
2: 84 percent / TFA / H2O / 2 h / 20 °C
3: 21 percent / NaH / tetrahydrofuran / 2 h / 60 °C
With sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water;
DOI:10.1039/b517572k
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