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(5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate

Base Information
  • Chemical Name:(5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate
  • CAS No.:1359014-82-6
  • Molecular Formula:C30H30N2O6S
  • Molecular Weight:546.644
  • Hs Code.:
(5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate

Synonyms:(5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate

Suppliers and Price of (5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate
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Chemical Property of (5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate
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Technology Process of (5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate

There total 5 articles about (5S,6S,Z)-methyl 13-(9H-fluoren-9-yl)-6-methyl-3,11-dioxo-1-phenyl-2,12-dioxa-7-thia-4,10-diazatridec-8-ene-5-carboxylate 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 bis(1,5-cyclooctadiene)nickel (0); copper(I) thiophene-2-carboxylate; triphenylphosphine; In 1,4-dioxane; at 50 ℃; for 3.5h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ol203399x
Guidance literature:
Multi-step reaction with 4 steps
1: tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate / ethyl acetate / 20 °C / Inert atmosphere
2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C / Inert atmosphere
3: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / ethyl acetate / 20 h / 20 °C / Inert atmosphere
4: copper(I) thiophene-2-carboxylate; bis(1,5-cyclooctadiene)nickel (0); triphenylphosphine / 1,4-dioxane / 3.5 h / 50 °C / Inert atmosphere
With bis(1,5-cyclooctadiene)nickel (0); copper(I) thiophene-2-carboxylate; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; tetra(n-butyl)ammonium hydrogensulfate; caesium carbonate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; In 1,4-dioxane; dichloromethane; ethyl acetate;
DOI:10.1021/ol203399x
Guidance literature:
Multi-step reaction with 2 steps
1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / ethyl acetate / 20 h / 20 °C / Inert atmosphere
2: copper(I) thiophene-2-carboxylate; bis(1,5-cyclooctadiene)nickel (0); triphenylphosphine / 1,4-dioxane / 3.5 h / 50 °C / Inert atmosphere
With bis(1,5-cyclooctadiene)nickel (0); copper(I) thiophene-2-carboxylate; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In 1,4-dioxane; ethyl acetate;
DOI:10.1021/ol203399x
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