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(3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester

Base Information
  • Chemical Name:(3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester
  • CAS No.:849372-28-7
  • Molecular Formula:C24H39NO7Si
  • Molecular Weight:481.662
  • Hs Code.:
(3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester

Synonyms:(3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester

Suppliers and Price of (3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester
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Chemical Property of (3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester
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Technology Process of (3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-carboxylic acid benzyl ester

There total 9 articles about (3aS,4R,7S,8S,8aR)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-7,8-dihydroxy-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]azepine-5-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 4 steps
1: 12 percent / NaBH(OAc)3; 4 Angstroem MS; AcOH / CH2Cl2 / 40 °C
2: 82 percent / KHCO3 / ethyl acetate; H2O
3: 99 percent / Grubbs' catalyst / CH2Cl2 / 24 h
4: 91 percent / OsO4; NMO / acetone; H2O
With osmium(VIII) oxide; N-methyl-2-indolinone; 4 Angstroem MS; sodium tris(acetoxy)borohydride; potassium hydrogencarbonate; acetic acid; Grubbs catalyst first generation; In dichloromethane; water; ethyl acetate; acetone;
DOI:10.3987/COM-04-S(P)45
Guidance literature:
Multi-step reaction with 7 steps
1: 92 percent / DIBAL-H / toluene / -40 °C
2: 77 percent / n-BuLi / tetrahydrofuran
3: 78 percent / PCC; 4 Angstroem MS / CH2Cl2
4: 12 percent / NaBH(OAc)3; 4 Angstroem MS; AcOH / CH2Cl2 / 40 °C
5: 82 percent / KHCO3 / ethyl acetate; H2O
6: 99 percent / Grubbs' catalyst / CH2Cl2 / 24 h
7: 91 percent / OsO4; NMO / acetone; H2O
With osmium(VIII) oxide; n-butyllithium; N-methyl-2-indolinone; 4 Angstroem MS; sodium tris(acetoxy)borohydride; diisobutylaluminium hydride; potassium hydrogencarbonate; acetic acid; pyridinium chlorochromate; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone; toluene; 2: Wittig reaction;
DOI:10.3987/COM-04-S(P)45
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