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Isoquinolinium,4a-(2,3-dimethoxyphenyl)-3,4,4a,5,6,7,8,8a-octahydro-2-methyl-6-oxo-,cis-, perchlorate

Base Information
  • Chemical Name:Isoquinolinium,4a-(2,3-dimethoxyphenyl)-3,4,4a,5,6,7,8,8a-octahydro-2-methyl-6-oxo-,cis-, perchlorate
  • CAS No.:91713-06-3
  • Molecular Formula:C18H24NO3.ClO4
  • Molecular Weight:401.844
  • Hs Code.:
Isoquinolinium,4a-(2,3-dimethoxyphenyl)-3,4,4a,5,6,7,8,8a-octahydro-2-methyl-6-oxo-,cis-, perchlorate

Synonyms:

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Chemical Property of Isoquinolinium,4a-(2,3-dimethoxyphenyl)-3,4,4a,5,6,7,8,8a-octahydro-2-methyl-6-oxo-,cis-, perchlorate
Chemical Property:
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Technology Process of Isoquinolinium,4a-(2,3-dimethoxyphenyl)-3,4,4a,5,6,7,8,8a-octahydro-2-methyl-6-oxo-,cis-, perchlorate

There total 12 articles about Isoquinolinium,4a-(2,3-dimethoxyphenyl)-3,4,4a,5,6,7,8,8a-octahydro-2-methyl-6-oxo-,cis-, perchlorate 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 12 steps
1: 1) n-BuLi, TMEDA / 1) hexane, ether, RT, 2 h, 2) RT, 18 h
2: 60 percent / 0.5 N H2SO4 / tetrahydrofuran / 20 h
3: p-toluenesulfonic acid monohydrate / benzene / 20 h / Heating
4: 1) BH3, 2) 3N NaOH, 30 percent H2O2 / 1) THF, RT, overnight, 2a) 1 h, RT, 2b) 45 deg C, overnight
5: 88 percent / pyridinium chlorochromate / CH2Cl2
6: 1) NaH / 1) DME, 2) toluene, 36 h, reflux
7: 1) OsO4, 2) NaIO4 / 1) ether, water, 20 min, 2) 48 h
8: 90 percent / NaH, t-amyl alcohol / benzene / 0.5 h / Heating
9: 99 percent / sodium acetate / ethanol / Heating
10: 60 percent / p-toluenesulfonyl chloride / pyridine; H2O / 0.75 h / Ambient temperature
11: 85 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
12: 91 percent / HClO4/HCl / diethyl ether; H2O; ethanol
With hydrogenchloride; sodium hydroxide; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; n-butyllithium; perchloric acid; tert-Amyl alcohol; N,N,N,N,-tetramethylethylenediamine; sulfuric acid; borane; dihydrogen peroxide; sodium acetate; sodium hydride; toluene-4-sulfonic acid; p-toluenesulfonyl chloride; pyridinium chlorochromate; In tetrahydrofuran; pyridine; diethyl ether; ethanol; dichloromethane; water; benzene;
DOI:10.1021/jo00194a026
Guidance literature:
Multi-step reaction with 10 steps
1: p-toluenesulfonic acid monohydrate / benzene / 20 h / Heating
2: 1) BH3, 2) 3N NaOH, 30 percent H2O2 / 1) THF, RT, overnight, 2a) 1 h, RT, 2b) 45 deg C, overnight
3: 88 percent / pyridinium chlorochromate / CH2Cl2
4: 1) NaH / 1) DME, 2) toluene, 36 h, reflux
5: 1) OsO4, 2) NaIO4 / 1) ether, water, 20 min, 2) 48 h
6: 90 percent / NaH, t-amyl alcohol / benzene / 0.5 h / Heating
7: 99 percent / sodium acetate / ethanol / Heating
8: 60 percent / p-toluenesulfonyl chloride / pyridine; H2O / 0.75 h / Ambient temperature
9: 85 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
10: 91 percent / HClO4/HCl / diethyl ether; H2O; ethanol
With hydrogenchloride; sodium hydroxide; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; perchloric acid; tert-Amyl alcohol; borane; dihydrogen peroxide; sodium acetate; sodium hydride; toluene-4-sulfonic acid; p-toluenesulfonyl chloride; pyridinium chlorochromate; In tetrahydrofuran; pyridine; diethyl ether; ethanol; dichloromethane; water; benzene;
DOI:10.1021/jo00194a026
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