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Fmoc-[D]Gly-OH

Base Information
  • Chemical Name:Fmoc-[D]Gly-OH
  • CAS No.:284665-11-8
  • Molecular Formula:C17H13 D2 N O4
  • Molecular Weight:299.295
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90583857
  • Wikidata:Q82475463
  • Mol file:284665-11-8.mol
Fmoc-[D]Gly-OH

Synonyms:284665-11-8;Fmoc-[D]Gly-OH;Fmoc-Gly-OH-2,2-d2;GLYCINE-2,2-D2-N-FMOC;2,2-dideuterio-2-(9H-fluoren-9-ylmethoxycarbonylamino)acetic acid;Fmoc-[D2]Gly-OH;Fmoc-[DGly-OH;Fmoc-Gly-OH-2,2 D2;SCHEMBL4656672;DTXSID90583857;HY-Y1250S2;MFCD01075436;Fmoc-Gly-OH-2,2-d2, 98 atom % D;MS-24305;CS-0226283;D99725;N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}(2,2-~2~H_2_)glycine

Suppliers and Price of Fmoc-[D]Gly-OH
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
  • TRC
  • N-Fmoc-glycine-d2
  • 10mg
  • $ 50.00
  • Sigma-Aldrich
  • Fmoc-Gly-OH-2,2-d2 98 atom % D
  • 1g
  • $ 793.00
  • Medical Isotopes, Inc.
  • Glycine-2,2-d2-N-t-FMOC
  • 0.5 g
  • $ 880.00
  • American Custom Chemicals Corporation
  • FMOC-GLY-OH-2,2-D2 95.00%
  • 5MG
  • $ 499.16
Total 8 raw suppliers
Chemical Property of Fmoc-[D]Gly-OH
Chemical Property:
  • Melting Point:174-175 °C(lit.)
     
  • PSA:75.63000 
  • LogP:3.00060 
  • Storage Temp.:2-8°C 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:299.11266145
  • Heavy Atom Count:22
  • Complexity:403
Purity/Quality:

97% *data from raw suppliers

N-Fmoc-glycine-d2 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCC(=O)O
  • Isomeric SMILES:[2H]C([2H])(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Uses Isotope labelled N-Fmoc-glycine is an N-Fmoc-protected form of Glycine (G615990). Glycine is a nonessential amino acid that acts as an inhibitory neyrotransmitter in the vertebrate central nervous system. Glycine also posesses cytoprotective against oxidant damage in the kidney.
Technology Process of Fmoc-[D]Gly-OH

There total 1 articles about Fmoc-[D]Gly-OH 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 1,4-dioxane; water;
DOI:10.1007/s13361-012-0540-6
Guidance literature:
Fmoc-α-d2-glycine; With 2,6-Dichlorobenzoyl chloride; Wang resin
With piperidine; Wang resin
N-(fluoren-9-ylmethoxycarbonyl)glycine; Fmoc-Leu-OH; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; Fmoc-Arg(Pg)-OH; Fmoc-Tyr(Pg)-OH; Further stages;
DOI:10.1007/s13361-012-0540-6
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