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FMOC-L-VALINE N-CARBOXY ANHYDRIDE

Base Information
  • Chemical Name:FMOC-L-VALINE N-CARBOXY ANHYDRIDE
  • CAS No.:129288-47-7
  • Molecular Formula:C21H19NO5
  • Molecular Weight:365.386
  • Hs Code.:2934999090
  • Mol file:129288-47-7.mol
FMOC-L-VALINE N-CARBOXY ANHYDRIDE

Synonyms:FMOC-L-VALINE N-CARBOXY ANHYDRIDE;Fmoc-Val-NCA;NALPHA-9-Fluorenylmethoxycarbonyl-L-valine N-carboxylic anhydride;FMOC-VALINE NCA;(S)-(9H-fluoren-9-yl)methyl 4-isopropyl-2,5-dioxooxazolidine-3-carboxylate

Suppliers and Price of FMOC-L-VALINE N-CARBOXY ANHYDRIDE
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
  • American Custom Chemicals Corporation
  • FMOC-VAL-NCA 95.00%
  • 5MG
  • $ 504.58
Total 10 raw suppliers
Chemical Property of FMOC-L-VALINE N-CARBOXY ANHYDRIDE
Chemical Property:
  • PSA:72.91000 
  • LogP:3.87680 
Purity/Quality:

98% *data from raw suppliers

FMOC-VAL-NCA 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of FMOC-L-VALINE N-CARBOXY ANHYDRIDE

There total 1 articles about FMOC-L-VALINE N-CARBOXY ANHYDRIDE 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 4-methyl-morpholine; In tetrahydrofuran; at 2 - 5 ℃; for 2h; Yield given;
DOI:10.1021/ja00176a063
Guidance literature:
Multi-step reaction with 8 steps
1: iPr2NEt / CH2Cl2
2: Et2NH / acetonitrile
3: iPr2NEt / CH2Cl2
4: Et2NH / acetonitrile
5: HOBt; EDC; iPr2NEt / CH2Cl2
6: HCl / dioxane
7: EDC; HOBt / CH2Cl2
8: DMP / CH2Cl2
With hydrogenchloride; phthalic acid dimethyl ester; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; diethylamine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2003.08.050
Guidance literature:
Multi-step reaction with 8 steps
1: iPr2NEt / CH2Cl2
2: Et2NH / acetonitrile
3: iPr2NEt / CH2Cl2
4: Et2NH / acetonitrile
5: HOBt; EDC; iPr2NEt / CH2Cl2
6: HCl / dioxane
7: EDC; HOBt / CH2Cl2
8: DMP / CH2Cl2
With hydrogenchloride; phthalic acid dimethyl ester; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; diethylamine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2003.08.050
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