Boc-DL-Glu(Obzl)-OH

Base Information

• Chemical Name: Boc-DL-Glu(Obzl)-OH
• CAS No.: 117997-81-6
• Molecular Formula: C17H23 N O6
• Molecular Weight: 337.373
• European Community (EC) Number: 874-551-8
• Nikkaji Number: J2.204.130D
• ChEMBL ID: CHEMBL2403046
• Mol file: 117997-81-6.mol

Synonyms:Boc-DL-Glu(Obzl)-OH;117997-81-6;5-(Benzyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid;2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid;Boc-DL-glutamic acid gamma-benzyl ester;MFCD00038258;MFCD00065569;SCHEMBL2009896;CHEMBL2403046;AJDUMMXHVCMISJ-UHFFFAOYSA-N;5-(benzyloxy)-2-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acid;MFCD00798612;AKOS022186438;boc-l-glutamic acid gamma-benzyl ester;FD21501;AS-10406;SY041312;SY041313;CS-0173368;FT-0629744;FT-0639281;EN300-6746817;4-Oxo-2-spiro(piperidine-4-yl)benzopyranhydrochloride;Z2044782738;2-tert-Butoxycarbonylamino-pentanedioic acid 5-benzyl ester;5-benzyloxy-2-(t-butoxycarbonylamino)-5-oxopentanoic acid

Chemical Property of Boc-DL-Glu(Obzl)-OH

Chemical Property:

• Boiling Point: 522.6±50.0 °C(Predicted)
• PKA: 3.81±0.10(Predicted)
• PSA: 101.93000
• Density: 1 +-.0.06 g/cm3(Predicted)
• LogP: 2.87880
• Storage Temp.: Store at RT.
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 10
• Exact Mass: 337.15253745
• Heavy Atom Count: 24
• Complexity: 437

Purity/Quality:

99% ^*data from raw suppliers

Boc-DL-Glu(OBzl)-OH ^*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)OCC1=CC=CC=C1)C(=O)O

Technology Process of Boc-DL-Glu(Obzl)-OH

There total 2 articles about Boc-DL-Glu(Obzl)-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:

Reference yield: 100.0%

di-tert-butyl dicarbonate (24424-99-5) + L-glutamic acid γ-benzyl ester (29456-09-5,25014-27-1) → 5-(benzyloxy)-2-(tert-butoxycarbonylamino)-5-oxopentanoic acid (117997-81-6)

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; at 45 ℃; for 3h;

DOI:10.1135/cccc19951765

Reference yield:

→ 5-(benzyloxy)-2-(tert-butoxycarbonylamino)-5-oxopentanoic acid (117997-81-6)

Guidance literature:

entspr.Dicyclohexylammoniumsalz, Citronensaeure;

DOI:10.1515/bchm2.1970.351.2.1576

Reference yield: 100.0%

DL-α,β-distearin (51063-97-9) + 5-(benzyloxy)-2-(tert-butoxycarbonylamino)-5-oxopentanoic acid (117997-81-6) → 5-benzyl 1-(2,3-bis(stearoyloxy)propyl) (tert-1-butoxycarbonyl)glutamate

Guidance literature:

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 16h;

upstream raw materials:

di-tert-butyl dicarbonate

L-glutamic acid γ-benzyl ester

Downstream raw materials:

2-[2-(4-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-butyrylamino)-3-(diphenoxy-phosphoryloxy)-propionylamino]-4-methyl-pentanoic acid benzyl ester

benzyl 4-((tert-butoxycarbonyl)amino)butanoate

N^α-Boc-ε-benzyl-DL-glutamic acid dipentylamide

4-nitrophenyl γ-benzyl-N-tert-butoxycarbonylglutamate

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