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3-Ethyl-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

Base Information
  • Chemical Name:3-Ethyl-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester
  • CAS No.:87238-30-0
  • Molecular Formula:C29H34N2O8
  • Molecular Weight:538.598
  • Hs Code.:
3-Ethyl-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

Synonyms:

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Chemical Property of 3-Ethyl-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester
Chemical Property:
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Technology Process of 3-Ethyl-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

There total 7 articles about 3-Ethyl-5-[3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl 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:
Multi-step reaction with 6 steps
1: 1.)isoamyl nitrite 2.)AcOH, NH4OAc, Zn / 1.)0 degC to room temp. 2.)CCl4 90-100 deg C, 3 h
2: 75 percent / Tl(III)nitrate trihydrate, HNO3 / methanol; CH2Cl2 / 24 h / Ambient temperature
3: 87.8 percent / Ac2O / acetic acid / 0.75 h / 80 °C
4: 1.)p-toluenesulphonic acid 2.)NaBH4 / 1.)CH2Cl2, MeOH 3 h 2.)CH2Cl2, MeOH NaBH4
5: 65 percent / BF3-etherate / nitromethane / 2 h / -15 °C
6: 1.)p-toluenesulphonic acid 2.)NaBH4 / 1.)MeOH 15 h, room temp. 2)MeOH
With sodium tetrahydroborate; boron trifluoride diethyl etherate; ammonium acetate; nitric acid; acetic anhydride; toluene-4-sulfonic acid; acetic acid; thallium(III) nitrate; zinc; isopentyl nitrite; In methanol; nitromethane; dichloromethane; acetic acid;
DOI:10.1016/S0040-4020(01)88706-8
Guidance literature:
Multi-step reaction with 5 steps
1: 75 percent / Tl(III)nitrate trihydrate, HNO3 / methanol; CH2Cl2 / 24 h / Ambient temperature
2: 87.8 percent / Ac2O / acetic acid / 0.75 h / 80 °C
3: 1.)p-toluenesulphonic acid 2.)NaBH4 / 1.)CH2Cl2, MeOH 3 h 2.)CH2Cl2, MeOH NaBH4
4: 65 percent / BF3-etherate / nitromethane / 2 h / -15 °C
5: 1.)p-toluenesulphonic acid 2.)NaBH4 / 1.)MeOH 15 h, room temp. 2)MeOH
With sodium tetrahydroborate; boron trifluoride diethyl etherate; nitric acid; acetic anhydride; toluene-4-sulfonic acid; thallium(III) nitrate; In methanol; nitromethane; dichloromethane; acetic acid;
DOI:10.1016/S0040-4020(01)88706-8
Guidance literature:
Multi-step reaction with 4 steps
1: 87.8 percent / Ac2O / acetic acid / 0.75 h / 80 °C
2: 1.)p-toluenesulphonic acid 2.)NaBH4 / 1.)CH2Cl2, MeOH 3 h 2.)CH2Cl2, MeOH NaBH4
3: 65 percent / BF3-etherate / nitromethane / 2 h / -15 °C
4: 1.)p-toluenesulphonic acid 2.)NaBH4 / 1.)MeOH 15 h, room temp. 2)MeOH
With sodium tetrahydroborate; boron trifluoride diethyl etherate; acetic anhydride; toluene-4-sulfonic acid; In nitromethane; acetic acid;
DOI:10.1016/S0040-4020(01)88706-8
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