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N-Carbomethoxy-L-tyrosine

Base Information Edit
  • Chemical Name:N-Carbomethoxy-L-tyrosine
  • CAS No.:338386-45-1
  • Molecular Formula:C11H13NO5
  • Molecular Weight:239.228
  • Hs Code.:
  • European Community (EC) Number:812-079-6
  • UNII:YLZ157AI2P
  • Wikidata:Q27896210
  • Mol file:338386-45-1.mol
N-Carbomethoxy-L-tyrosine

Synonyms:N-Carbomethoxy-L-tyrosine;338386-45-1;YLZ157AI2P;Tyrosine, N-(methoxycarbonyl)-;N-Carbomethoxy tyrosine, (+)-;L-Tyrosine, N-(methoxycarbonyl)-;UNII-YLZ157AI2P;(2S)-3-(4-hydroxyphenyl)-2-(methoxycarbonylamino)propanoic Acid;(2s)-3-(4-Hydroxyphenyl)-2-[(methoxycarbonyl)amino]propanoic acid;SCHEMBL3389559;CS-0259862;EN300-7430850;Q27896210

Suppliers and Price of N-Carbomethoxy-L-tyrosine
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 5 raw suppliers
Chemical Property of N-Carbomethoxy-L-tyrosine Edit
Chemical Property:
  • XLogP3:0.4
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:5
  • Exact Mass:239.07937252
  • Heavy Atom Count:17
  • Complexity:273
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC(=O)NC(CC1=CC=C(C=C1)O)C(=O)O
  • Isomeric SMILES:COC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O
Technology Process of N-Carbomethoxy-L-tyrosine

There total 1 articles about N-Carbomethoxy-L-tyrosine 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 sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃;
DOI:10.1021/ol015526i DOI:10.1021/ja016030z
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