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L-VALINYL-L-LEUCINYL ANILIDE

Base Information
  • Chemical Name:L-VALINYL-L-LEUCINYL ANILIDE
  • CAS No.:874945-31-0
  • Molecular Formula:C17H27N3O2
  • Molecular Weight:305.42
  • Hs Code.:
  • Mol file:874945-31-0.mol
L-VALINYL-L-LEUCINYL ANILIDE

Synonyms:L-VALINYL-L-LEUCINYL ANILIDE;Val-L-leu-anilide;L-Valyl-N-phenyl-L-leucinamide

Suppliers and Price of L-VALINYL-L-LEUCINYL ANILIDE
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
  • Usbiological
  • L-Valinyl-L-leucinyl Anilide
  • 5mg
  • $ 460.00
  • TRC
  • L-Valinyl-L-leucinylAnilide
  • 50mg
  • $ 1320.00
  • Medical Isotopes, Inc.
  • L-Valinyl-L-leucinylAnilide
  • 5 mg
  • $ 900.00
  • Medical Isotopes, Inc.
  • L-Valinyl-L-leucinylAnilide
  • 25 mg
  • $ 2200.00
  • American Custom Chemicals Corporation
  • L-VALINYL-L-LEUCINYL ANILIDE 95.00%
  • 50MG
  • $ 1963.50
  • American Custom Chemicals Corporation
  • L-VALINYL-L-LEUCINYL ANILIDE 95.00%
  • 5MG
  • $ 345.40
Total 2 raw suppliers
Chemical Property of L-VALINYL-L-LEUCINYL ANILIDE
Chemical Property:
  • PSA:84.22000 
  • LogP:3.30350 
  • Solubility.:DMF, DMSO 
Purity/Quality:

95% *data from raw suppliers

L-Valinyl-L-leucinyl Anilide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses L-Valinyl-L-leucinyl Anilide is used as biomarkers for the quantification of hemoglobin adducts to toxic electrophiles.
Technology Process of L-VALINYL-L-LEUCINYL ANILIDE

There total 6 articles about L-VALINYL-L-LEUCINYL ANILIDE 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 carbonate; In ethyl acetate;
DOI:10.1002/ejoc.200500429
Guidance literature:
Multi-step reaction with 2 steps
1: 100 percent / hydrogen chloride / CH2Cl2; ethyl acetate
2: aq. Na2CO3 / ethyl acetate
With hydrogenchloride; sodium carbonate; In dichloromethane; ethyl acetate;
DOI:10.1002/ejoc.200500429
Guidance literature:
Multi-step reaction with 5 steps
1.1: HOAt; iPr2NEt; EDC*HCl / CH2Cl2 / 1 h / 0 °C
1.2: 65 percent / CH2Cl2 / 20 °C
2.1: 98 percent / hydrogen chloride / CH2Cl2; ethyl acetate
3.1: HOAt; iPr2NEt; EDC*HCl / CH2Cl2 / 1 h / 0 °C
3.2: 91 percent / CH2Cl2 / 20 °C
4.1: 100 percent / hydrogen chloride / CH2Cl2; ethyl acetate
5.1: aq. Na2CO3 / ethyl acetate
With hydrogenchloride; 1-hydroxy-7-aza-benzotriazole; sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; ethyl acetate;
DOI:10.1002/ejoc.200500429
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