C₂₆H₃₆N₂O₅

Base Information

Chemical Name:C₂₆H₃₆N₂O₅
CAS No.:145387-90-2
Molecular Formula:C₂₆H₃₆N₂O₅
Molecular Weight:456.582
Hs Code.:

C<sub>26</sub>H<sub>36</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:C₂₆H₃₆N₂O₅

Suppliers and Price of C₂₆H₃₆N₂O₅

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₂₆H₃₆N₂O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₆H₃₆N₂O₅

There total 17 articles about C₂₆H₃₆N₂O₅ 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:

Reference yield: 72.0%

: 145387-89-9
(1aS,3R,3aS,7aR,7bR)-3-Methoxymethoxy-6-(4-methoxy-phenyl)-7a-[(Z)-(S)-1-(2-trimethylsilanyl-ethanesulfonyl)-1,2,5,6,7,8-hexahydro-azocin-2-ylmethyl]-octahydro-1-oxa-6-aza-cyclopropa[a]naphthalen-7-one

: 145387-90-2
C₂₆H₃₆N₂O₅

Guidance literature:: With cesium fluoride; In N,N-dimethyl-formamide; Heating;
DOI:10.1016/S0040-4039(00)60944-9

Reference yield:

: 124981-58-4
1-(2-Methoxy-ethyl)-cyclohexa-2,5-dienecarboxylic acid

: 145387-90-2
C₂₆H₃₆N₂O₅

Guidance literature:: Multi-step reaction with 17 steps

1: 1) (PhO)2P(=O)N₃, Et₃N, pyrrolidine; 2) I₂, H₂O / 2) THF

2: 2,2'-azobisisobutyronitrile / benzene / Ambient temperature

4: 4-(N,N-dimethylamino)pyridine, pyridine

6: BBr₃

7: Swern oxidation

9: 68 percent / H₂, pyridine / BaSO₄

10: 86 percent / Ph₃P, diethyl azodicarboxylate

11: (CH₃)3SiCl, NaI / acetonitrile

12: Et₃N, 4-(N,N-dimethylamino)pyridine / CH₂Cl₂

13: 91 percent / KH, 18-crown-6, tetra-n-butylammonium iodide

14: LiOH

15: VO(acac)2, t-BuOOH / Heating

16: 86 percent / Hunig's base

17: 72 percent / CsF / dimethylformamide / Heating

With pyrrolidine; pyridine; tert.-butylhydroperoxide; dmap; lithium hydroxide; chloro-trimethyl-silane; bis(acetylacetonate)oxovanadium; 18-crown-6 ether; 2,2'-azobis(isobutyronitrile); diphenyl phosphoryl azide; water; hydrogen; iodine; boron tribromide; tetra-(n-butyl)ammonium iodide; potassium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; cesium fluoride; sodium iodide; diethylazodicarboxylate; barium sulfate; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1016/S0040-4039(00)60944-9

Reference yield:

: 145387-74-2
(1R,5R,8R)-8-Iodo-1-(2-methoxy-ethyl)-6-oxa-bicyclo[3.2.1]oct-2-en-7-one

: 145387-90-2
C₂₆H₃₆N₂O₅

Guidance literature:: Multi-step reaction with 16 steps

1: 2,2'-azobisisobutyronitrile / benzene / Ambient temperature

3: 4-(N,N-dimethylamino)pyridine, pyridine

5: BBr₃

6: Swern oxidation

8: 68 percent / H₂, pyridine / BaSO₄

9: 86 percent / Ph₃P, diethyl azodicarboxylate

10: (CH₃)3SiCl, NaI / acetonitrile

11: Et₃N, 4-(N,N-dimethylamino)pyridine / CH₂Cl₂

12: 91 percent / KH, 18-crown-6, tetra-n-butylammonium iodide

13: LiOH

14: VO(acac)2, t-BuOOH / Heating

15: 86 percent / Hunig's base

16: 72 percent / CsF / dimethylformamide / Heating

With pyridine; tert.-butylhydroperoxide; dmap; lithium hydroxide; chloro-trimethyl-silane; bis(acetylacetonate)oxovanadium; 18-crown-6 ether; 2,2'-azobis(isobutyronitrile); hydrogen; boron tribromide; tetra-(n-butyl)ammonium iodide; potassium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; cesium fluoride; sodium iodide; diethylazodicarboxylate; barium sulfate; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1016/S0040-4039(00)60944-9