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4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde

Base Information
  • Chemical Name:4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde
  • CAS No.:107223-34-7
  • Molecular Formula:C18H17NO3
  • Molecular Weight:295.338
  • Hs Code.:
4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde

Synonyms:4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde

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Chemical Property of 4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde
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Technology Process of 4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde

There total 11 articles about 4-<(4-cyanophenoxy)methyl>-2-hydroxy-3-propylbenzaldehyde 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 10 steps
1: 2.) H2 / 2.) 5percent Pd/C / 1.) water, EtOH, 40 deg C, 4 h, 2.) water, EtOH, 60 psi, 16 h
2: 1.) n-BuLi / 1.) hexane, THF, 4 h, 2.) hexane, THF, 25 deg C, 20 h
3: 77 percent / HOAc, 48percent aq. HBr / 24 h / Heating
4: triethylamine / CH2Cl2 / 16 h
5: 1.) NaOEt, 2.) NaI / 1.) EtOH, 0.25 h, 0 deg C, 2.) EtOH, RT, 48 h
6: NH4OH / ethanol / 4 h
7: 86 percent / H2O / 24 h / Heating
8: 97 percent / pyridine, 4-(dimethylamino)pyridine / CH2Cl2 / 3 h
9: ethyl chloroformate / toluene / 16 h / Ambient temperature
10: 1.) 2-nitropropane Na salt, 2.) dimethylamine / 1.) EtOH, reflux, 4 h, 2.) MeCN, 48 h
With pyridine; dmap; ammonium hydroxide; n-butyllithium; hydrogen bromide; hydrogen; sodium ethanolate; chloroformic acid ethyl ester; sodium 2-nitropropane; acetic acid; dimethyl amine; triethylamine; sodium iodide; palladium on activated charcoal; In ethanol; dichloromethane; water; toluene;
DOI:10.1021/jm00388a028
Guidance literature:
Multi-step reaction with 9 steps
1: 1.) n-BuLi / 1.) hexane, THF, 4 h, 2.) hexane, THF, 25 deg C, 20 h
2: 77 percent / HOAc, 48percent aq. HBr / 24 h / Heating
3: triethylamine / CH2Cl2 / 16 h
4: 1.) NaOEt, 2.) NaI / 1.) EtOH, 0.25 h, 0 deg C, 2.) EtOH, RT, 48 h
5: NH4OH / ethanol / 4 h
6: 86 percent / H2O / 24 h / Heating
7: 97 percent / pyridine, 4-(dimethylamino)pyridine / CH2Cl2 / 3 h
8: ethyl chloroformate / toluene / 16 h / Ambient temperature
9: 1.) 2-nitropropane Na salt, 2.) dimethylamine / 1.) EtOH, reflux, 4 h, 2.) MeCN, 48 h
With pyridine; dmap; ammonium hydroxide; n-butyllithium; hydrogen bromide; sodium ethanolate; chloroformic acid ethyl ester; sodium 2-nitropropane; acetic acid; dimethyl amine; triethylamine; sodium iodide; In ethanol; dichloromethane; water; toluene;
DOI:10.1021/jm00388a028
Guidance literature:
Multi-step reaction with 6 steps
1: 1.) NaOEt, 2.) NaI / 1.) EtOH, 0.25 h, 0 deg C, 2.) EtOH, RT, 48 h
2: NH4OH / ethanol / 4 h
3: 86 percent / H2O / 24 h / Heating
4: 97 percent / pyridine, 4-(dimethylamino)pyridine / CH2Cl2 / 3 h
5: ethyl chloroformate / toluene / 16 h / Ambient temperature
6: 1.) 2-nitropropane Na salt, 2.) dimethylamine / 1.) EtOH, reflux, 4 h, 2.) MeCN, 48 h
With pyridine; dmap; ammonium hydroxide; sodium ethanolate; chloroformic acid ethyl ester; sodium 2-nitropropane; dimethyl amine; sodium iodide; In ethanol; dichloromethane; water; toluene;
DOI:10.1021/jm00388a028
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