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2-benzyloxycarbonylacetyl-7,12,18-triethyl-3,8,13,17-tetramethylporphyrin

Base Information Edit
  • Chemical Name:2-benzyloxycarbonylacetyl-7,12,18-triethyl-3,8,13,17-tetramethylporphyrin
  • CAS No.:76044-26-3
  • Molecular Formula:C40H42N4O3
  • Molecular Weight:626.798
  • Hs Code.:
  • Mol file:76044-26-3.mol
2-benzyloxycarbonylacetyl-7,12,18-triethyl-3,8,13,17-tetramethylporphyrin

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Chemical Property of 2-benzyloxycarbonylacetyl-7,12,18-triethyl-3,8,13,17-tetramethylporphyrin Edit
Chemical Property:
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Technology Process of 2-benzyloxycarbonylacetyl-7,12,18-triethyl-3,8,13,17-tetramethylporphyrin

There total 8 articles about 2-benzyloxycarbonylacetyl-7,12,18-triethyl-3,8,13,17-tetramethylporphyrin 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: 6 g / hydrochloric acid / ethanol / 2 h / Heating
2: 1.) sodium hydroxide, 2.) acetic acid / 1.) ethanol, 3.5 h, 2.) ethanol, water, 0 deg C, 1 h
3: 2.) benzoyl chloride / 1.) reflux, 30 min, 2.) from 0 deg C to RT
4: 245 mg / trifluoroacetic acid / methanol / 1.) 0 deg C, 20 min, 2.) heating, overnight
5: 227 mg / pyridine, potassium hydroxide / methanol / 3 h / Heating
6: oxalyl chloride / CH2Cl2 / 0.42 h / Heating
7: 1.) isopropylmagnesium bromide / 1.) tetrahydrofuran, reflux, 5 min, 2.) 5 min
With pyridine; hydrogenchloride; potassium hydroxide; sodium hydroxide; oxalyl dichloride; isopropylmagnesium bromide; benzoyl chloride; acetic acid; trifluoroacetic acid; In methanol; ethanol; dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1: 2.) benzoyl chloride / 1.) reflux, 30 min, 2.) from 0 deg C to RT
2: 245 mg / trifluoroacetic acid / methanol / 1.) 0 deg C, 20 min, 2.) heating, overnight
3: 227 mg / pyridine, potassium hydroxide / methanol / 3 h / Heating
4: oxalyl chloride / CH2Cl2 / 0.42 h / Heating
5: 1.) isopropylmagnesium bromide / 1.) tetrahydrofuran, reflux, 5 min, 2.) 5 min
With pyridine; potassium hydroxide; oxalyl dichloride; isopropylmagnesium bromide; benzoyl chloride; trifluoroacetic acid; In methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 6 steps
1: 1.) sodium hydroxide, 2.) acetic acid / 1.) ethanol, 3.5 h, 2.) ethanol, water, 0 deg C, 1 h
2: 2.) benzoyl chloride / 1.) reflux, 30 min, 2.) from 0 deg C to RT
3: 245 mg / trifluoroacetic acid / methanol / 1.) 0 deg C, 20 min, 2.) heating, overnight
4: 227 mg / pyridine, potassium hydroxide / methanol / 3 h / Heating
5: oxalyl chloride / CH2Cl2 / 0.42 h / Heating
6: 1.) isopropylmagnesium bromide / 1.) tetrahydrofuran, reflux, 5 min, 2.) 5 min
With pyridine; potassium hydroxide; sodium hydroxide; oxalyl dichloride; isopropylmagnesium bromide; benzoyl chloride; acetic acid; trifluoroacetic acid; In methanol; dichloromethane;
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