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Fmoc-Sar-OH

Base Information Edit
  • Chemical Name:Fmoc-Sar-OH
  • CAS No.:77128-70-2
  • Molecular Formula:C18H17NO4
  • Molecular Weight:311.337
  • Hs Code.:2924 29 70
  • European Community (EC) Number:674-628-4
  • Nikkaji Number:J1.399.415C
  • Mol file:77128-70-2.mol
Fmoc-Sar-OH

Synonyms:Fmoc-Sar-OH;77128-70-2;Fmoc-sarcosine;2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]acetic acid;[(9h-fluoren-9-ylmethoxycarbonyl)methylamino]acetic acid;Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-;N-Alpha-(9-Fluorenylmethyloxycarbonyl)-N-Alpha-Methyl-Glycine;Fmoc-Nalpha-methylglycine;2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetic acid;2-({[(9H-FLUOREN-9-YL)METHOXY]CARBONYL}(METHYL)AMINO)ACETIC ACID;fmoc-n-me-gly-oh;MFCD00151926;n-fmoc-n-methylglycine;Fmoc-Sar-OH. H2O;N-Methyl-N-Fmoc-Gly-OH;SCHEMBL119579;n-[(9h-fluoren-9-ylmethoxy)carbonyl]-n-methylglycine;Fmoc-Sar-OH, >=98.0%;AKOS009157239;CS-W012058;DS-9904;HY-W011342;F1163;FT-0641635;nalpha-(9-fluorenylmethoxycarbonyl)-sarcosine;n-alpha-(9-fluorenylmethoxycarbonyl)-sarcosine;EN300-624013;H10706;n-alpha-(9-fluorenylmethyloxycarbonyl)-sarcosine;A838964;Q-101727;N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-methylglycine;Z1123720000;[(9H-Fluoren-9-ylmethoxycarbonyl)-methyl-amino]-acetic acid Fmoc-Sar-OH

Suppliers and Price of Fmoc-Sar-OH
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
  • Usbiological
  • Fmoc-N-methylglycine
  • 10g
  • $ 379.00
  • TRC
  • Fmoc-Sar-OH
  • 1g
  • $ 75.00
  • TCI Chemical
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methylglycine >98.0%(HPLC)(T)
  • 5g
  • $ 41.00
  • TCI Chemical
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methylglycine >98.0%(HPLC)(T)
  • 25g
  • $ 123.00
  • SynQuest Laboratories
  • Fmoc-Sar-OH
  • 100 g
  • $ 152.00
  • Sigma-Aldrich
  • Fmoc-Sar-OH Novabiochem?
  • 25 g
  • $ 214.00
  • Sigma-Aldrich
  • Fmoc-Sar-OH Novabiochem . CAS 77128-70-2, molar mass 311.33 g/mol., Novabiochem
  • 8520550025
  • $ 207.00
  • Sigma-Aldrich
  • Fmoc-Sar-OH ≥98.0%
  • 5 g
  • $ 129.00
  • Sigma-Aldrich
  • Fmoc-Sar-OH ≥98.0%
  • 5g-f
  • $ 129.00
  • Sigma-Aldrich
  • Fmoc-Sar-OH Novabiochem?
  • 5 g
  • $ 59.20
Total 68 raw suppliers
Chemical Property of Fmoc-Sar-OH Edit
Chemical Property:
  • Vapor Pressure:2.44E-11mmHg at 25°C 
  • Melting Point:117.0 to 121.0 °C 
  • Refractive Index:1.615 
  • Boiling Point:512.8 °C at 760 mmHg 
  • PKA:3.91±0.10(Predicted) 
  • Flash Point:263.9 °C 
  • PSA:66.84000 
  • Density:1.292 g/cm3 
  • LogP:2.95190 
  • Storage Temp.:2-8°C 
  • Solubility.:Soluble in DMF. 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:311.11575802
  • Heavy Atom Count:23
  • Complexity:430
Purity/Quality:

99% *data from raw suppliers

Fmoc-N-methylglycine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(CC(=O)O)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Uses N-Fmoc-N-methylglycine is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Technology Process of Fmoc-Sar-OH

There total 6 articles about Fmoc-Sar-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; at 20 ℃; for 5h;
DOI:10.1016/j.tet.2018.09.011
Guidance literature:
With triethylsilane; aluminium trichloride; In chloroform; at 20 ℃;
DOI:10.1021/jo050916u
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