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Boc-glu(ome)-OH

Base Information Edit
  • Chemical Name:Boc-glu(ome)-OH
  • CAS No.:45214-91-3
  • Molecular Formula:C11H19NO6
  • Molecular Weight:261.275
  • Hs Code.:2924199090
  • European Community (EC) Number:863-129-9
  • DSSTox Substance ID:DTXSID20427018
  • Nikkaji Number:J949.208I
  • Wikidata:Q72449417
  • ChEMBL ID:CHEMBL1222061
  • Mol file:45214-91-3.mol
Boc-glu(ome)-OH

Synonyms:BOC-GLU(OME)-OH;45214-91-3;(S)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid;Boc-L-Glutamic acid gamma-methyl ester;(2S)-5-methoxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid;(S)-2-(tert-butoxycarbonylamino)-5-methoxy-5-oxopentanoic acid;N-Boc-L-glutamic acid 5-methyl ester;MFCD00190794;SCHEMBL384624;CHEMBL1222061;DTXSID20427018;OHYMUFVCRVPMEY-ZETCQYMHSA-N;AMY25476;N-[(1,1-dimethylethoxy)carbonyl]-L-glutamic acid 5-methyl ester;AKOS015950980;CS-W005143;FD21381;HY-W005143;AS-19046;BP-12380;PD196432;EN300-1090628;A847899;N-t-butoxycarbonyl-l-glutamic acid 5-methyl ester;N-tert-Butoxycarbonylglutamic acid ?-methyl ester;J-300095;Q-101682;N-(tert-Butoxycarbonyl)-L-glutamic acid=gamma-methyl;(2S)-2-[(tert-butoxycarbonyl)amino]-5-methoxy-5-oxopentanoic acid;N-[(1,1-dimethylethoxy)carbonyl]-L-glutamic acid-5-methyl ester;(25)-2-[(tert-butoxy)carbonylamino]-4-(methoxycarbonyl)butanoic acid;(2S)-2-[(tert-Butoxy)carbonylamino]-4-(methoxycarbonyl)butanoic acid;(2S)-2-{[(tert-butoxy)carbonyl]amino}-5-methoxy-5-oxopentanoic acid

Suppliers and Price of Boc-glu(ome)-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
  • Boc-L-glutamic acid gamma-methyl ester
  • 500mg
  • $ 375.00
  • TRC
  • N-Boc-L-glutamicAcid5-MethylEster
  • 10g
  • $ 150.00
  • Crysdot
  • (S)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoicacid 97%
  • 1000g
  • $ 495.00
  • Crysdot
  • (S)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoicacid 97%
  • 500g
  • $ 297.00
  • ChemScene
  • (S)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoicacid ≥98.0%
  • 500g
  • $ 295.00
  • ChemScene
  • (S)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoicacid ≥98.0%
  • 100g
  • $ 73.00
  • ChemPep
  • Boc-Glu(OMe)-OH ≥98%
  • 100g
  • $ 867.00
  • ChemPep
  • Boc-Glu(OMe)-OH ≥98%
  • 25g
  • $ 315.00
  • Biosynth Carbosynth
  • Boc-L-glutamic acid gamma-methyl ester
  • 50 g
  • $ 70.00
  • Biosynth Carbosynth
  • Boc-Glu(OMe)-OH
  • 5 g
  • $ 79.00
Total 86 raw suppliers
Chemical Property of Boc-glu(ome)-OH Edit
Chemical Property:
  • Melting Point:119-123 °C 
  • Boiling Point:428.35 °C at 760 mmHg 
  • PKA:3.82±0.10(Predicted) 
  • Flash Point:212.859 °C 
  • PSA:101.93000 
  • Density:1.183 g/cm3 
  • LogP:1.30840 
  • Storage Temp.:2-8°C 
  • Solubility.:Chloroform (Sparingly), Methanol (Slightly) 
  • XLogP3:0.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:8
  • Exact Mass:261.12123733
  • Heavy Atom Count:18
  • Complexity:320
Purity/Quality:

98%min *data from raw suppliers

Boc-L-glutamic acid gamma-methyl ester *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NC(CCC(=O)OC)C(=O)O
  • Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CCC(=O)OC)C(=O)O
  • Uses N-Boc-L-glutamic Acid 5-Methyl Ester is an intermediate used in the synthesis of Isodesmosine Chloride Hydrate (Synthetic) (I815051), which is a component of elastin and also it is extremely hygroscopic and must be stored over a desiccant such as silica gel.
Technology Process of Boc-glu(ome)-OH

There total 19 articles about Boc-glu(ome)-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 triethylamine; In 1,4-dioxane; water; at 20 ℃; for 18h;
Guidance literature:
With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; for 2h; under 2068.65 Torr;
DOI:10.1039/b702076g
Guidance literature:
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ol500333t
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