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FMoc-(S)-3-AMino-5-hexynoic acid

Base Information
  • Chemical Name:FMoc-(S)-3-AMino-5-hexynoic acid
  • CAS No.:1217669-02-7
  • Molecular Formula:C21H19NO4
  • Molecular Weight:349.37986
  • Hs Code.:
  • Mol file:1217669-02-7.mol
FMoc-(S)-3-AMino-5-hexynoic acid

Synonyms:(S)-3-{[((9H-fluoren-9-yl)methoxy)carbonyl]amino}hex-5-ynoic acid;Fmoc-L-β3-Pra-OH;

Suppliers and Price of FMoc-(S)-3-AMino-5-hexynoic acid
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
  • Matrix Scientific
  • Fmoc-(S)-3-amino-5-hexynoic acid
  • 1g
  • $ 814.00
  • Matrix Scientific
  • Fmoc-(S)-3-amino-5-hexynoic acid
  • 250mg
  • $ 300.00
  • Crysdot
  • (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hex-5-ynoicacid 95+%
  • 5g
  • $ 2376.00
  • Crysdot
  • (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hex-5-ynoicacid 95+%
  • 1g
  • $ 589.00
  • Chemenu
  • (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)hex-5-ynoicacid 95%
  • 500mg
  • $ 147.00
  • Chemenu
  • (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)hex-5-ynoicacid 95%
  • 250mg
  • $ 92.00
  • Alichem
  • (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hex-5-ynoicacid
  • 5g
  • $ 2514.75
  • Alichem
  • (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hex-5-ynoicacid
  • 1g
  • $ 630.70
Total 5 raw suppliers
Chemical Property of FMoc-(S)-3-AMino-5-hexynoic acid
Chemical Property:
  • PSA:75.63000 
  • LogP:3.78260 
Purity/Quality:

97% *data from raw suppliers

Fmoc-(S)-3-amino-5-hexynoic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of FMoc-(S)-3-AMino-5-hexynoic acid

There total 4 articles about FMoc-(S)-3-AMino-5-hexynoic acid 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 silver trifluoroacetate; In tetrahydrofuran; water; at 20 ℃; for 8h; Inert atmosphere; Darkness; Sonication;
DOI:10.1055/s-0032-1317445 DOI:10.1055/s-0032-1317445
Guidance literature:
Multi-step reaction with 3 steps
1.1: potassium carbonate / water; 1,4-dioxane / 0.5 h / 0 °C / Inert atmosphere
2.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.5 h / -20 °C / Inert atmosphere
2.2: 1.5 h / -20 - 0 °C / Inert atmosphere
3.1: silver trifluoroacetate / water; tetrahydrofuran / 8 h / 20 °C / Inert atmosphere; Darkness; Sonication
With 4-methyl-morpholine; silver trifluoroacetate; potassium carbonate; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane; water; 3.1: |Arndt-Eistert Homologation;
DOI:10.1055/s-0032-1317445 DOI:10.1055/s-0032-1317445
Guidance literature:
Multi-step reaction with 3 steps
1.1: potassium carbonate / water; 1,4-dioxane / 0.5 h / 0 °C / Inert atmosphere
2.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.5 h / -20 °C / Inert atmosphere
2.2: 1.5 h / -20 - 0 °C / Inert atmosphere
3.1: silver trifluoroacetate / water; tetrahydrofuran / 8 h / 20 °C / Inert atmosphere; Darkness; Sonication
With 4-methyl-morpholine; silver trifluoroacetate; potassium carbonate; isobutyl chloroformate; In tetrahydrofuran; 1,4-dioxane; water; 3.1: |Arndt-Eistert Homologation;
DOI:10.1055/s-0032-1317445 DOI:10.1055/s-0032-1317445
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