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

Encyclopedia

Methyl n-formyl-3-methoxy-o-methyltyrosinate

Base Information Edit
  • Chemical Name:Methyl n-formyl-3-methoxy-o-methyltyrosinate
  • CAS No.:58143-18-3
  • Molecular Formula:C13H17NO5
  • Molecular Weight:267.2778
  • Hs Code.:
  • NSC Number:121979
  • DSSTox Substance ID:DTXSID20298245
  • Mol file:58143-18-3.mol
Methyl n-formyl-3-methoxy-o-methyltyrosinate

Synonyms:58143-18-3;methyl n-formyl-3-methoxy-o-methyltyrosinate;NSC121979;DTXSID20298245;NSC-121979

Suppliers and Price of Methyl n-formyl-3-methoxy-o-methyltyrosinate
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
Total 2 raw suppliers
Chemical Property of Methyl n-formyl-3-methoxy-o-methyltyrosinate Edit
Chemical Property:
  • Vapor Pressure:1.09E-08mmHg at 25°C 
  • Boiling Point:461.2°Cat760mmHg 
  • Flash Point:232.8°C 
  • Density:1.163g/cm3 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:267.11067264
  • Heavy Atom Count:19
  • Complexity:297
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)CC(C(=O)OC)NC=O)OC
Technology Process of Methyl n-formyl-3-methoxy-o-methyltyrosinate

There total 2 articles about Methyl n-formyl-3-methoxy-o-methyltyrosinate 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 2 steps
1: acetic acid anhydride
With acetic anhydride;
DOI:10.1021/jo01109a019
Post RFQ for Price