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Methionylphenylalanine

Base Information Edit
  • Chemical Name:Methionylphenylalanine
  • CAS No.:14492-14-9
  • Molecular Formula:C14H20N2O3S
  • Molecular Weight:296.39
  • Hs Code.:2930909090
  • NSC Number:322477
  • DSSTox Substance ID:DTXSID40932452
  • Mol file:14492-14-9.mol
Methionylphenylalanine

Synonyms:Met-Phe;methionylphenylalanine

Suppliers and Price of Methionylphenylalanine
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
  • TRC
  • H-Met-Phe-OH
  • 50mg
  • $ 90.00
  • American Custom Chemicals Corporation
  • MET-PHE-OH 98.00%
  • 5G
  • $ 1992.38
Total 16 raw suppliers
Chemical Property of Methionylphenylalanine Edit
Chemical Property:
  • Vapor Pressure:2.62E-13mmHg at 25°C 
  • Boiling Point:558.5°Cat760mmHg 
  • Flash Point:291.5°C 
  • PSA:117.72000 
  • Density:1.233g/cm3 
  • LogP:1.97010 
  • Storage Temp.:-15°C 
  • XLogP3:-1.7
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:8
  • Exact Mass:296.11946368
  • Heavy Atom Count:20
  • Complexity:320
Purity/Quality:

99% *data from raw suppliers

H-Met-Phe-OH *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CSCCC(C(=O)NC(CC1=CC=CC=C1)C(=O)O)N
  • Recent ClinicalTrials:A Comparative Study of Mometasone Furoate Nasal Spray and Fluticasone Propionate Nasal Spray in Patients With Perennial Allergic Rhinitis (Study P04512)
  • Recent EU Clinical Trials:Evaluation of the anti-inflammatory effects of glycopyrronium added to indacaterol/mometasone on the allergen-induced late asthmatic response
Technology Process of Methionylphenylalanine

There total 2 articles about Methionylphenylalanine 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 aminolysin-A; In water; dimethyl sulfoxide; at 50 ℃; for 6h; pH=8; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1039/c0ob00403k
Guidance literature:
Multi-step reaction with 2 steps
1: S9-ACAP / water; dimethyl sulfoxide / 0.5 h / 65 °C / pH 6.4 / aq. buffer; Enzymatic reaction
2: aminolysin-A / water; dimethyl sulfoxide / 6 h / 50 °C / pH 8 / aq. phosphate buffer; Enzymatic reaction
With aminolysin-A; S9-ACAP; In water; dimethyl sulfoxide;
DOI:10.1039/c0ob00403k
Guidance literature:
Multi-step reaction with 3 steps
1: aq. NaOH / 0 - 20 °C / pH 10.5
2: aq. HCl / 12 h / Heating
3: aq. H2O2 / methanol / -20 °C
With hydrogenchloride; sodium hydroxide; dihydrogen peroxide; In methanol;
DOI:10.1139/v02-025
upstream raw materials:

Met-OMe

L-phenylalanine

L-phenylalanine-p-nitroanilide

Downstream raw materials:

N-MOC-Met-Phe-OMe

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