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FMOC-4-AMINO-3-METHOXYBENZOIC ACID

Base Information Edit
  • Chemical Name:FMOC-4-AMINO-3-METHOXYBENZOIC ACID
  • CAS No.:254737-60-5
  • Molecular Formula:C23H19NO5
  • Molecular Weight:389.408
  • Hs Code.:
  • Mol file:254737-60-5.mol
FMOC-4-AMINO-3-METHOXYBENZOIC ACID

Synonyms:

Suppliers and Price of FMOC-4-AMINO-3-METHOXYBENZOIC ACID
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Matrix Scientific
  • Fmoc-4-amino-3-methoxybenzoic acid
  • 1g
  • $ 356.00
  • Matrix Scientific
  • Fmoc-4-amino-3-methoxybenzoic acid
  • 5g
  • $ 1302.00
  • Crysdot
  • 4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methoxybenzoicacid 97%
  • 5g
  • $ 903.00
  • American Custom Chemicals Corporation
  • FMOC-4-AMINO-3-METHOXYBENZOIC ACID 95.00%
  • 1G
  • $ 639.45
Total 5 raw suppliers
Chemical Property of FMOC-4-AMINO-3-METHOXYBENZOIC ACID Edit
Chemical Property:
Purity/Quality:

98%min *data from raw suppliers

Fmoc-4-amino-3-methoxybenzoic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of FMOC-4-AMINO-3-METHOXYBENZOIC ACID

There total 1 articles about FMOC-4-AMINO-3-METHOXYBENZOIC ACID 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:
In tetrahydrofuran; chloroform; at 60 ℃; for 12h;
DOI:10.3390/ijms22115482
Guidance literature:
Multi-step reaction with 4 steps
1.1: thionyl chloride / 5 h / Reflux
2.1: pyridine / acetone / 8 h / 0 - 20 °C
3.1: diethylamine / N,N-dimethyl-formamide / 5 h / 20 °C
4.1: pyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / 1 h
4.2: 8 h / 20 °C
With pyridine; thionyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diethylamine; In N,N-dimethyl-formamide; acetone;
DOI:10.3390/ijms22115482
Guidance literature:
Multi-step reaction with 3 steps
1: thionyl chloride / 5 h / Reflux
2: pyridine / acetone / 8 h / 0 - 20 °C
3: diethylamine / N,N-dimethyl-formamide / 5 h / 20 °C
With pyridine; thionyl chloride; diethylamine; In N,N-dimethyl-formamide; acetone;
DOI:10.3390/ijms22115482
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