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Benzoic acid, 2-heptyl-4-[3-heptyl-5-hydroxy-2-(methoxycarbonyl)phenoxy]-3,6-dimeth oxy-, methyl ester

Base Information Edit
  • Chemical Name:Benzoic acid, 2-heptyl-4-[3-heptyl-5-hydroxy-2-(methoxycarbonyl)phenoxy]-3,6-dimeth oxy-, methyl ester
  • CAS No.:94693-39-7
  • Molecular Formula:C32H46O8
  • Molecular Weight:558.712
  • Hs Code.:
  • Mol file:94693-39-7.mol
Benzoic acid,
2-heptyl-4-[3-heptyl-5-hydroxy-2-(methoxycarbonyl)phenoxy]-3,6-dimeth
oxy-, methyl ester

Synonyms:

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Chemical Property of Benzoic acid, 2-heptyl-4-[3-heptyl-5-hydroxy-2-(methoxycarbonyl)phenoxy]-3,6-dimeth oxy-, methyl ester Edit
Chemical Property:
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Technology Process of Benzoic acid, 2-heptyl-4-[3-heptyl-5-hydroxy-2-(methoxycarbonyl)phenoxy]-3,6-dimeth oxy-, methyl ester

There total 4 articles about Benzoic acid, 2-heptyl-4-[3-heptyl-5-hydroxy-2-(methoxycarbonyl)phenoxy]-3,6-dimeth oxy-, methyl 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: 96 percent / K2CO3 / acetone / 3 h / Heating
2: 90 percent / H2 / 10percent Pd/C / ethyl acetate / 6 h
3: 78 percent / K2CO3 / 2-methyl-propan-2-ol / 16 h / Heating
4: 1.) Br2, AcOH, 2.) HBr / 1.) CCl4, Ac2O, a) RT, 0.5 h, b) reflux, 3 h 2.) CCl4, AcOH, H2O, reflux, 2 h
With hydrogen bromide; hydrogen; bromine; potassium carbonate; acetic acid; palladium on activated charcoal; In ethyl acetate; acetone; tert-butyl alcohol;
DOI:10.1071/CH9842349
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / H2 / 10percent Pd/C / ethyl acetate / 6 h
2: 78 percent / K2CO3 / 2-methyl-propan-2-ol / 16 h / Heating
3: 1.) Br2, AcOH, 2.) HBr / 1.) CCl4, Ac2O, a) RT, 0.5 h, b) reflux, 3 h 2.) CCl4, AcOH, H2O, reflux, 2 h
With hydrogen bromide; hydrogen; bromine; potassium carbonate; acetic acid; palladium on activated charcoal; In ethyl acetate; tert-butyl alcohol;
DOI:10.1071/CH9842349
Guidance literature:
Multi-step reaction with 2 steps
1: 78 percent / K2CO3 / 2-methyl-propan-2-ol / 16 h / Heating
2: 1.) Br2, AcOH, 2.) HBr / 1.) CCl4, Ac2O, a) RT, 0.5 h, b) reflux, 3 h 2.) CCl4, AcOH, H2O, reflux, 2 h
With hydrogen bromide; bromine; potassium carbonate; acetic acid; In tert-butyl alcohol;
DOI:10.1071/CH9842349
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