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5-benzyloxycarbonyl-12,18-diethyl-7-methoxycarbonyl-2,2,8,13,17-pentamethylchlorin

Base Information
  • Chemical Name:5-benzyloxycarbonyl-12,18-diethyl-7-methoxycarbonyl-2,2,8,13,17-pentamethylchlorin
  • CAS No.:79264-63-4
  • Molecular Formula:C39H42N4O4
  • Molecular Weight:630.787
  • Hs Code.:
5-benzyloxycarbonyl-12,18-diethyl-7-methoxycarbonyl-2,2,8,13,17-pentamethylchlorin

Synonyms:

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Chemical Property of 5-benzyloxycarbonyl-12,18-diethyl-7-methoxycarbonyl-2,2,8,13,17-pentamethylchlorin
Chemical Property:
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Technology Process of 5-benzyloxycarbonyl-12,18-diethyl-7-methoxycarbonyl-2,2,8,13,17-pentamethylchlorin

There total 26 articles about 5-benzyloxycarbonyl-12,18-diethyl-7-methoxycarbonyl-2,2,8,13,17-pentamethylchlorin 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 10 steps
1: 1.) sodium nitrite, 2.) zinc dust, sodium acetate / 1.) water, glacial acetic acid, 20 deg C, overnight, 2.) 70 - 80 deg C, 1 h
2: 94 percent / H2 / palladium on charcoal / methanol; tetrahydrofuran / 5 h
3: 88 percent / aq. sodium hydrogen carbonate, iodine, potassium iodide / CHCl3; H2O / 0.25 h
4: H2, sodium acetate / palladium on charcoal / methanol / 6 h
5: 68.4 percent / sulphuric acid / tetrahydrofuran / 24 h / 20 °C
6: 67.4 percent / toluene-p-sulphonic acid / CH2Cl2 / 0.17 h
7: trifluoroacetic acid / 0.17 h
8: methanol; trifluoroacetic acid / 0.75 h
9: 76.7 percent Turnov. / CH2Cl2 / 1 h
10: 1.) hydrated copper(II) acetate, DBU, 2.) hydrogen sulphide / 1.) acetonitrile, reflux, 4 h, 2.) TFA, 22 h
With sulfuric acid; hydrogen sulfide; hydrogen; iodine; copper diacetate; sodium acetate; sodium hydrogencarbonate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide; zinc; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; trifluoroacetic acid;
DOI:10.1039/P19840002733
Guidance literature:
Multi-step reaction with 7 steps
1: H2, sodium acetate / palladium on charcoal / methanol / 6 h
2: 68.4 percent / sulphuric acid / tetrahydrofuran / 24 h / 20 °C
3: 67.4 percent / toluene-p-sulphonic acid / CH2Cl2 / 0.17 h
4: trifluoroacetic acid / 0.17 h
5: methanol; trifluoroacetic acid / 0.75 h
6: 76.7 percent Turnov. / CH2Cl2 / 1 h
7: 1.) hydrated copper(II) acetate, DBU, 2.) hydrogen sulphide / 1.) acetonitrile, reflux, 4 h, 2.) TFA, 22 h
With sulfuric acid; hydrogen sulfide; hydrogen; copper diacetate; sodium acetate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; trifluoroacetic acid;
DOI:10.1039/P19840002733
Guidance literature:
Multi-step reaction with 8 steps
1: 88 percent / aq. sodium hydrogen carbonate, iodine, potassium iodide / CHCl3; H2O / 0.25 h
2: H2, sodium acetate / palladium on charcoal / methanol / 6 h
3: 68.4 percent / sulphuric acid / tetrahydrofuran / 24 h / 20 °C
4: 67.4 percent / toluene-p-sulphonic acid / CH2Cl2 / 0.17 h
5: trifluoroacetic acid / 0.17 h
6: methanol; trifluoroacetic acid / 0.75 h
7: 76.7 percent Turnov. / CH2Cl2 / 1 h
8: 1.) hydrated copper(II) acetate, DBU, 2.) hydrogen sulphide / 1.) acetonitrile, reflux, 4 h, 2.) TFA, 22 h
With sulfuric acid; hydrogen sulfide; hydrogen; iodine; copper diacetate; sodium acetate; sodium hydrogencarbonate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; trifluoroacetic acid;
DOI:10.1039/P19840002733
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