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Fmoc-D-phenylalanine

Base Information Edit
  • Chemical Name:Fmoc-D-phenylalanine
  • CAS No.:86123-10-6
  • Molecular Formula:C24H21NO4
  • Molecular Weight:387.435
  • Hs Code.:29242990
  • European Community (EC) Number:630-426-8
  • Nikkaji Number:J860.962D
  • ChEMBL ID:CHEMBL348015
  • Mol file:86123-10-6.mol
Fmoc-D-phenylalanine

Synonyms:Fmoc-D-phenylalanine;Fmoc-D-Phe-OH;86123-10-6;N-Fmoc-D-phenylalanine;(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylpropanoic acid;CHEMBL348015;D-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-;N-(9-FLUORENYLMETHOXYCARBONYL)-D-PHENYLALANINE;MFCD00062955;(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-phenylpropanoic acid;Fmoc-DPhe-OH;D-Fmoc-Phenylalanine;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine;Fmoc--cyclohexyl-D-Ala-OH;SCHEMBL118169;SJVFAHZPLIXNDH-JOCHJYFZSA-N;Fmoc-D-Phe-OH, >=98.0%;BDBM50121969;AKOS015837405;AM82157;CS-W011742;DS-1654;HY-W011026;DCSD 002855 (1);AC-24163;F0605;EN300-649822;F11068;M03371;A841564;AU-004/43510613;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]phenylalanine;J-300208;(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-phenylalanine;Z1723944681;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-PHENYLALANINE;(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenyl-propanoate;(r)-3-phenyl-2-(9h-fluoren-9-ylmethoxycarbonylamino)-propionic acid;(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)-amino)-3-phenylpropanoic acid;(R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-phenylpropanoic acid

Suppliers and Price of Fmoc-D-phenylalanine
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
  • Acrotein
  • Fmoc-D-phenylalanine 97%
  • 5g
  • $ 13.02
  • Acrotein
  • Fmoc-D-phenylalanine 97%
  • 250g
  • $ 229.17
  • Activate Scientific
  • Fmoc-D-Phe-OH 98% ee
  • 100 g
  • $ 167.00
  • Activate Scientific
  • Fmoc-D-Phe-OH 98% ee
  • 5 g
  • $ 20.00
  • Activate Scientific
  • Fmoc-D-Phe-OH 98% ee
  • 25 g
  • $ 53.00
  • AHH
  • Fmoc-D-Phenylalanine 98%
  • 500g
  • $ 678.00
  • AK Scientific
  • Fmoc-D-phenylalanine
  • 25g
  • $ 34.00
  • AK Scientific
  • Fmoc-D-phenylalanine
  • 100g
  • $ 101.00
  • Alfa Aesar
  • N-Fmoc-D-phenylalanine, 98%
  • 5g
  • $ 79.90
  • Alfa Aesar
  • N-Fmoc-D-phenylalanine, 98%
  • 25g
  • $ 253.00
Total 139 raw suppliers
Chemical Property of Fmoc-D-phenylalanine Edit
Chemical Property:
  • Appearance/Colour:white powder 
  • Vapor Pressure:3.07E-16mmHg at 25°C 
  • Melting Point:181-185 °C 
  • Refractive Index:38 ° (C=1, DMF) 
  • Boiling Point:620.1 °C at 760 mmHg 
  • PKA:3.77±0.10(Predicted) 
  • Flash Point:328.8 °C 
  • PSA:75.63000 
  • Density:1.276 g/cm3 
  • LogP:4.61190 
  • Storage Temp.:2-8°C 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:387.14705815
  • Heavy Atom Count:29
  • Complexity:551
Purity/Quality:

99.0% Min *data from raw suppliers

Fmoc-D-phenylalanine 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
  • Isomeric SMILES:C1=CC=C(C=C1)C[C@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
  • Uses N-Fmoc-D-phenylalanine is an N-Fmoc-protected form of D-Phenylalanine (P319410). D-Phenylalanine is an essential amino acid that serves as a primary precursor for the biosynthesis of catecholamines in the body. D-Phenylalanine is also known to antagonize stress-induced analgesia in humans, and also acts as an anti-enkephalinase agent.
Technology Process of Fmoc-D-phenylalanine

There total 9 articles about Fmoc-D-phenylalanine 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 hydrogencarbonate; In acetone; Ambient temperature;
Guidance literature:
With sodium carbonate; In 1,4-dioxane; water; at 0 - 20 ℃; for 7h;
DOI:10.1093/nar/gky1211
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