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BOC-Met-AnpGlu ethylene dithioketal Ile-OCH3

Base Information
  • Chemical Name:BOC-Met-AnpGlu ethylene dithioketal Ile-OCH3
  • CAS No.:174464-43-8
  • Molecular Formula:C31H49N3O7S3
  • Molecular Weight:671.944
  • Hs Code.:
BOC-Met-An<sup>p</sup>Glu ethylene dithioketal Ile-OCH<sub>3</sub>

Synonyms:BOC-Met-AnpGlu ethylene dithioketal Ile-OCH3

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Chemical Property of BOC-Met-AnpGlu ethylene dithioketal Ile-OCH3
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Technology Process of BOC-Met-AnpGlu ethylene dithioketal Ile-OCH3

There total 7 articles about BOC-Met-AnpGlu ethylene dithioketal Ile-OCH3 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 7 steps
1: 79 percent / triflic acid / CH2Cl2 / 1 h / Ambient temperature
2: 49 percent / BF3*Et2O / 1) 0 deg C, 15 min; 2) rt, 2 h
3: 90 percent / HCl / ethyl acetate; CH2Cl2 / 16 h / Ambient temperature
4: 92 percent / Et3N / tetrahydrofuran; H2O / 17 h / Ambient temperature
5: 1.) carbonylbis(3-methylimidazolium triflate), 2.) N-methylmorpholine / 1) THF, MeNO2, 5 min; 2) THF, MeNO2, rt, 2 h
6: 93 percent / HCl / ethyl acetate / 3 h / Ambient temperature
7: 1.) methyl triflate, CDI, N-methylimidazole, 2.) N-methylmorpholine / 1) THF, MeNO2, 0 deg C, 8 min; 2) THF, DMF, rt, 3 h
With 4-methyl-morpholine; 1-methyl-1H-imidazole; hydrogenchloride; trifluorormethanesulfonic acid; boron trifluoride diethyl etherate; 1,1'-carbonylbis(3-methyl-1H-imidazol-3-ium) triflate; triethylamine; 1,1'-carbonyldiimidazole; methyl trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane; water; ethyl acetate;
DOI:10.1021/jo951754c
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) carbonylbis(3-methylimidazolium triflate), 2.) N-methylmorpholine / 1) THF, MeNO2, 5 min; 2) THF, MeNO2, rt, 2 h
2: 93 percent / HCl / ethyl acetate / 3 h / Ambient temperature
3: 1.) methyl triflate, CDI, N-methylimidazole, 2.) N-methylmorpholine / 1) THF, MeNO2, 0 deg C, 8 min; 2) THF, DMF, rt, 3 h
With 4-methyl-morpholine; 1-methyl-1H-imidazole; hydrogenchloride; 1,1'-carbonylbis(3-methyl-1H-imidazol-3-ium) triflate; 1,1'-carbonyldiimidazole; methyl trifluoromethanesulfonate; In ethyl acetate;
DOI:10.1021/jo951754c
Guidance literature:
Multi-step reaction with 5 steps
1: 90 percent / HCl / ethyl acetate; CH2Cl2 / 16 h / Ambient temperature
2: 92 percent / Et3N / tetrahydrofuran; H2O / 17 h / Ambient temperature
3: 1.) carbonylbis(3-methylimidazolium triflate), 2.) N-methylmorpholine / 1) THF, MeNO2, 5 min; 2) THF, MeNO2, rt, 2 h
4: 93 percent / HCl / ethyl acetate / 3 h / Ambient temperature
5: 1.) methyl triflate, CDI, N-methylimidazole, 2.) N-methylmorpholine / 1) THF, MeNO2, 0 deg C, 8 min; 2) THF, DMF, rt, 3 h
With 4-methyl-morpholine; 1-methyl-1H-imidazole; hydrogenchloride; 1,1'-carbonylbis(3-methyl-1H-imidazol-3-ium) triflate; triethylamine; 1,1'-carbonyldiimidazole; methyl trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane; water; ethyl acetate;
DOI:10.1021/jo951754c
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