Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester

Base Information
  • Chemical Name:N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester
  • CAS No.:56724-14-2
  • Molecular Formula:C19H21NO5
  • Molecular Weight:343.379
  • Hs Code.:
  • DSSTox Substance ID:DTXSID501232366
N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester

Synonyms:N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester;DTXSID501232366;56724-14-2

Suppliers and Price of N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester
Supply Marketing:
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
Total 0 raw suppliers
Chemical Property of N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester
Chemical Property:
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:8
  • Exact Mass:343.14197277
  • Heavy Atom Count:25
  • Complexity:424
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=CC(=CC(=C1)CC(C(=O)OC)NC(=O)C2=CC=CC=C2)OC
Technology Process of N-Benzoyl-3,5-dimethoxyphenylalanine methyl ester

There total 4 articles about N-Benzoyl-3,5-dimethoxyphenylalanine 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:
With hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; acetic acid; for 10h; under 3102.89 Torr;
DOI:10.1016/S0040-4020(00)00470-1
Guidance literature:
Multi-step reaction with 3 steps
1: 86 percent / sodium acetate / acetic anhydride / 2.5 h / 85 °C
2: 88 percent / Na2CO3 / 0.75 h / Heating
3: H2 / 10 percent Pd/C / tetrahydrofuran; methanol; acetic acid / 10 h / 3102.89 Torr
With hydrogen; sodium acetate; sodium carbonate; palladium on activated charcoal; In tetrahydrofuran; methanol; acetic anhydride; acetic acid; 1: Condensation / 2: Ring cleavage / 3: Catalytic hydrogenation;
DOI:10.1016/S0040-4020(00)00470-1
Guidance literature:
Multi-step reaction with 3 steps
1: 86 percent / sodium acetate / acetic anhydride / 2.5 h / 85 °C
2: 88 percent / Na2CO3 / 0.75 h / Heating
3: H2 / 10 percent Pd/C / tetrahydrofuran; methanol; acetic acid / 10 h / 3102.89 Torr
With hydrogen; sodium acetate; sodium carbonate; palladium on activated charcoal; In tetrahydrofuran; methanol; acetic anhydride; acetic acid; 1: Condensation / 2: Ring cleavage / 3: Catalytic hydrogenation;
DOI:10.1016/S0040-4020(00)00470-1
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 56724-14-2