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Tyrosyl-alanyl-delta-phenylalanyl-glycinamide

Base Information
  • Chemical Name:Tyrosyl-alanyl-delta-phenylalanyl-glycinamide
  • CAS No.:97992-01-3
  • Molecular Formula:C23H29N5O5
  • Molecular Weight:455.514
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60243355
  • Wikidata:Q83127433
  • Mol file:97992-01-3.mol
Tyrosyl-alanyl-delta-phenylalanyl-glycinamide

Synonyms:TA-delta-Phe-GNH2;Tyr-Ala-delta-Phe-GlyNH2;tyrosyl-alanyl-delta-phenylalanyl-glycinamide

Suppliers and Price of Tyrosyl-alanyl-delta-phenylalanyl-glycinamide
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 1 raw suppliers
Chemical Property of Tyrosyl-alanyl-delta-phenylalanyl-glycinamide
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:920.7°C at 760 mmHg 
  • PKA:9.97±0.15(Predicted) 
  • Flash Point:510.6°C 
  • Density:1.289g/cm3 
  • XLogP3:-0.5
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:11
  • Exact Mass:455.21686904
  • Heavy Atom Count:33
  • Complexity:674
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C(=O)NC(CC1=CC=CC=C1)C(=O)NCC(=O)N)NC(=O)C(CC2=CC=C(C=C2)O)N
  • Isomeric SMILES:C[C@H](C(=O)N[C@H](CC1=CC=CC=C1)C(=O)NCC(=O)N)NC(=O)[C@H](CC2=CC=C(C=C2)O)N
Technology Process of Tyrosyl-alanyl-delta-phenylalanyl-glycinamide

There total 4 articles about Tyrosyl-alanyl-delta-phenylalanyl-glycinamide 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: isobutylchloroformate, N-methylmorpholine, NH3 / tetrahydrofuran / 1.) 1 h, -10 deg C, 2.) 1-2 h, 0-10 deg C
2: aqueous 90percent trifluoroacetic acid, anisole / 0.5 h
With 4-methyl-morpholine; ammonia; methoxybenzene; trifluoroacetic acid; isobutyl chloroformate; In tetrahydrofuran;
Guidance literature:
Multi-step reaction with 2 steps
1: 10percent Pd/C (HCOONH4) / methanol; acetic acid / 0.25 h
2: TFA-CH2Cl2-anisole (5:4:1) / 0.5 h / Ambient temperature
With Pd/C (HCOONH4); trifluoroacetic acid; In methanol; acetic acid;
DOI:10.1016/S0040-4039(00)94583-0
Guidance literature:
With methoxybenzene; trifluoroacetic acid; for 0.5h; Yield given;
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