1499-55-4,MFCD00002632
Catalog No.:AA003R74

1499-55-4 | L-Glutamic acid 5-methyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$7.00   $5.00
- +
25g
97%
in stock  
$12.00   $8.00
- +
100g
97%
in stock  
$19.00   $14.00
- +
500g
97%
in stock  
$94.00   $66.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003R74
Chemical Name:
L-Glutamic acid 5-methyl ester
CAS Number:
1499-55-4
Molecular Formula:
C6H11NO4
Molecular Weight:
161.1558
MDL Number:
MFCD00002632
SMILES:
COC(=O)CCC(C(=O)O)N
Properties
Properties
 
BP:
316.1°C at 760 mmHg  
Form:
Solid  
MP:
182 °C (dec.);(lit.);  
Refractive Index:
29 ° (C=2, 6mol/L HCl)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
157  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-3.4  

Upstream Synthesis Route

[1]YakugakuZasshi,1953,vol.73,p.397

[2]Chem.Abstr.,1954,p.2597

[1]Patent:US2016/16890,2016,A1,.Locationinpatent:Paragraph0163

[2]BioorganicandMedicinalChemistryLetters,2007,vol.17,#13,p.3793-3797

[3]TetrahedronLetters,2010,vol.51,#9,p.1333-1335

[4]Synthesis,1987,#7,p.635-637

[5]OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85

[6]Patent:WO2004/50084,2004,A2,.Locationinpatent:Page/Pagecolumn57;58

[7]HelveticaChimicaActa,1955,vol.38,p.1491,1499

[8]TetrahedronLetters,2003,vol.44,#28,p.5251-5253

[9]JournaloftheChemicalSociety,1951,p.2294

[10]BiochemicalPreparations,1957,vol.5,p.79,82

[11]JournaloftheChemicalSociety,ChemicalCommunications,1988,#12,p.828-829

[12]JournaloftheChemicalSociety,1950,p.3239,3243

[13]TetrahedronLetters,2000,vol.41,#32,p.6191-6194

[14]TetrahedronAsymmetry,2000,vol.11,#24,p.4965-4973

[15]OrganicandBiomolecularChemistry,2006,vol.4,#9,p.1796-1805

[16]ChemSusChem,2011,vol.4,#6,p.785-791

[17]Chemistry-AEuropeanJournal,2013,vol.19,#21,p.6824-6830

[18]OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85

[19]Patent:US2561323,1948,,

[1]Patent:US2016/16890,2016,A1,.Locationinpatent:Paragraph0159-0162

[1]OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85

[2]JournalofOrganicChemistry,1975,vol.40,p.3287-3288

[3]JournaloftheChemicalSociety,ChemicalCommunications,1986,#20,p.1514-1516

[1]Tetrahedron,2000,vol.56,#46,p.9093-9102

Downstream Synthesis Route

[1]CurrentPatentAssignee:OTSUKAHOLDINGSCOLTD-US2016/16890,2016,A1Locationinpatent:Paragraph0163

[2]More,SwatiS.;Vince,Robert[BioorganicandMedicinalChemistryLetters,2007,vol.17,#13,p.3793-3797]

[3]Locationinpatent:schemeortableMollica,Adriano;Stefanucci,Azzurra;Feliciani,Federica;Torino,Domenica;Cacciatore,Ivana;Pinnen,Francesco;Lucente,Gino[TetrahedronLetters,2010,vol.51,#9,p.1333-1335]

[4]Albert,Rainer;Danklmaier,Johann;Hoenig,Helmut;Kandolf,Harald[Synthesis,1987,#7,p.635-637]

[5]CurrentPatentAssignee:AUROBINDOPHARMALIMITED-WO2022/13706,2022,A1Locationinpatent:Page/Pagecolumn14;15

[6]Ager,DavidJ.;Babler,Scott;Erickson,RobertA.;Froen,DianeE.;Kittleson,Jeannine;Pantaleone,DavidP.;Prakash,Indra;Zhi,Ben[OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85]

[7]CurrentPatentAssignee:HEBREWUNIVERSITYOFJERUSALEM;YissumResearch&Development(in:HebrewUniversity)-WO2004/50084,2004,A2Locationinpatent:Page/Pagecolumn57;58

[8]Boissonnasetal.[HelveticaChimicaActa,1955,vol.38,p.1491,1499]Bhat,RamakrishnaG.;Porhiel,Emmanuel;Saravanan,Vadivelu;Chandrasekaran,Srinivasan[TetrahedronLetters,2003,vol.44,#28,p.5251-5253]

[9]Coleman[JournaloftheChemicalSociety,1951,p.2294]Lepp;Dunn[BiochemicalPreparations,1957,vol.5,p.79,82]Baldwin,JackE.;North,Michael;Flinn,Anthony;Moloney,MarkG.[JournaloftheChemicalSociety.Chemicalcommunications,1988,#12,p.828-829]

[10]Hanbyetal.[JournaloftheChemicalSociety,1950,p.3239,3243]

[11]Balayiannis;Karigiannis;Gatos;Papaioannou;DeClercq[TetrahedronLetters,2000,vol.41,#32,p.6191-6194]

[12]Luesch,Hendrik;Uzar,HorstC.[TetrahedronAsymmetry,2000,vol.11,#24,p.4965-4973]

[13]Hjelmgaard,Thomas;Tanner,David[OrganicandBiomolecularChemistry,2006,vol.4,#9,p.1796-1805]

[14]Locationinpatent:schemeortableLammens,TijsM.;Nôtre,Jér̂meLe;Franssen,MauriceC.R.;Scott,ElinorL.;Sanders,JohanP.M.[ChemSusChem,2011,vol.4,#6,p.785-791]

[15]Arthur,IsaacN.;Hennessy,JamesE.;Padmakshan,Dharshana;Stigers,DannonJ.;Lesturgez,Stéphanie;Fraser,SamuelA.;Liutkus,Mantas;Otting,Gottfried;Oakeshott,JohnG.;Easton,ChristopherJ.[Chemistry-AEuropeanJournal,2013,vol.19,#21,p.6824-6830]

[16]Ager,DavidJ.;Babler,Scott;Erickson,RobertA.;Froen,DianeE.;Kittleson,Jeannine;Pantaleone,DavidP.;Prakash,Indra;Zhi,Ben[OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85]

[17]CurrentPatentAssignee:PFIZERINC-US2561323,1948,A

[1]NipponKagakuZasshi,1959,vol.80,p.492,494    Chem.Abstr.,1961,p.3452

[2]JournaloftheChemicalSociety,1950,p.3239,3243

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1953,vol.73,p.397    Chem.Abstr.,1954,p.2597

[1]Miroshnikov,A.I.etal.[JournalofgeneralchemistryoftheUSSR,1970,vol.40,#2,p.395-407][ZhurnalObshcheiKhimii,1970,vol.40,#2,p.429-443]

[1]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.451-454    ZhurnalObshcheiKhimii,1970,vol.40,p.487-491

[2]AustralianJournalofChemistry,1965,vol.18,p.1095-1103

Literature
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SDS
Tags:1499-55-4 Molecular Formula|1499-55-4 MDL|1499-55-4 SMILES|1499-55-4 L-Glutamic acid 5-methyl ester
Catalog No.: AA003R74
1499-55-4,MFCD00002632
1499-55-4 | L-Glutamic acid 5-methyl ester
Pack Size: 5g
Purity: 97%
in stock
$7.00 $5.00
Pack Size: 25g
Purity: 97%
in stock
$12.00 $8.00
Pack Size: 100g
Purity: 97%
in stock
$19.00 $14.00
Pack Size: 500g
Purity: 97%
in stock
$94.00 $66.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003R74
Chemical Name: L-Glutamic acid 5-methyl ester
CAS Number: 1499-55-4
Molecular Formula: C6H11NO4
Molecular Weight: 161.1558
MDL Number: MFCD00002632
SMILES: COC(=O)CCC(C(=O)O)N
Properties
BP: 316.1°C at 760 mmHg  
Form: Solid  
MP: 182 °C (dec.);(lit.);  
Refractive Index: 29 ° (C=2, 6mol/L HCl)  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 157  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -3.4  
Upstream Synthesis Route
67-56-1    4124-76-9    6384-08-3    1499-55-4 

[1]YakugakuZasshi,1953,vol.73,p.397

[2]Chem.Abstr.,1954,p.2597

67-56-1    56-86-0    1499-55-4 

[1]Patent:US2016/16890,2016,A1,.Locationinpatent:Paragraph0163

[2]BioorganicandMedicinalChemistryLetters,2007,vol.17,#13,p.3793-3797

[3]TetrahedronLetters,2010,vol.51,#9,p.1333-1335

[4]Synthesis,1987,#7,p.635-637

[5]OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85

[6]Patent:WO2004/50084,2004,A2,.Locationinpatent:Page/Pagecolumn57;58

[7]HelveticaChimicaActa,1955,vol.38,p.1491,1499

[8]TetrahedronLetters,2003,vol.44,#28,p.5251-5253

[9]JournaloftheChemicalSociety,1951,p.2294

[10]BiochemicalPreparations,1957,vol.5,p.79,82

[11]JournaloftheChemicalSociety,ChemicalCommunications,1988,#12,p.828-829

[12]JournaloftheChemicalSociety,1950,p.3239,3243

[13]TetrahedronLetters,2000,vol.41,#32,p.6191-6194

[14]TetrahedronAsymmetry,2000,vol.11,#24,p.4965-4973

[15]OrganicandBiomolecularChemistry,2006,vol.4,#9,p.1796-1805

[16]ChemSusChem,2011,vol.4,#6,p.785-791

[17]Chemistry-AEuropeanJournal,2013,vol.19,#21,p.6824-6830

[18]OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85

[19]Patent:US2561323,1948,,

67-56-1    138-15-8    1499-55-4 

[1]Patent:US2016/16890,2016,A1,.Locationinpatent:Paragraph0159-0162

6525-53-7    1499-55-4 

[1]OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85

[2]JournalofOrganicChemistry,1975,vol.40,p.3287-3288

[3]JournaloftheChemicalSociety,ChemicalCommunications,1986,#20,p.1514-1516

56-86-0    75-36-5    1499-55-4 

[1]Tetrahedron,2000,vol.56,#46,p.9093-9102

Downstream Synthesis Route
67-56-1    56-86-0    1499-55-4 

[1]CurrentPatentAssignee:OTSUKAHOLDINGSCOLTD-US2016/16890,2016,A1Locationinpatent:Paragraph0163

[2]More,SwatiS.;Vince,Robert[BioorganicandMedicinalChemistryLetters,2007,vol.17,#13,p.3793-3797]

[3]Locationinpatent:schemeortableMollica,Adriano;Stefanucci,Azzurra;Feliciani,Federica;Torino,Domenica;Cacciatore,Ivana;Pinnen,Francesco;Lucente,Gino[TetrahedronLetters,2010,vol.51,#9,p.1333-1335]

[4]Albert,Rainer;Danklmaier,Johann;Hoenig,Helmut;Kandolf,Harald[Synthesis,1987,#7,p.635-637]

[5]CurrentPatentAssignee:AUROBINDOPHARMALIMITED-WO2022/13706,2022,A1Locationinpatent:Page/Pagecolumn14;15

[6]Ager,DavidJ.;Babler,Scott;Erickson,RobertA.;Froen,DianeE.;Kittleson,Jeannine;Pantaleone,DavidP.;Prakash,Indra;Zhi,Ben[OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85]

[7]CurrentPatentAssignee:HEBREWUNIVERSITYOFJERUSALEM;YissumResearch&Development(in:HebrewUniversity)-WO2004/50084,2004,A2Locationinpatent:Page/Pagecolumn57;58

[8]Boissonnasetal.[HelveticaChimicaActa,1955,vol.38,p.1491,1499]Bhat,RamakrishnaG.;Porhiel,Emmanuel;Saravanan,Vadivelu;Chandrasekaran,Srinivasan[TetrahedronLetters,2003,vol.44,#28,p.5251-5253]

[9]Coleman[JournaloftheChemicalSociety,1951,p.2294]Lepp;Dunn[BiochemicalPreparations,1957,vol.5,p.79,82]Baldwin,JackE.;North,Michael;Flinn,Anthony;Moloney,MarkG.[JournaloftheChemicalSociety.Chemicalcommunications,1988,#12,p.828-829]

[10]Hanbyetal.[JournaloftheChemicalSociety,1950,p.3239,3243]

[11]Balayiannis;Karigiannis;Gatos;Papaioannou;DeClercq[TetrahedronLetters,2000,vol.41,#32,p.6191-6194]

[12]Luesch,Hendrik;Uzar,HorstC.[TetrahedronAsymmetry,2000,vol.11,#24,p.4965-4973]

[13]Hjelmgaard,Thomas;Tanner,David[OrganicandBiomolecularChemistry,2006,vol.4,#9,p.1796-1805]

[14]Locationinpatent:schemeortableLammens,TijsM.;Nôtre,Jér̂meLe;Franssen,MauriceC.R.;Scott,ElinorL.;Sanders,JohanP.M.[ChemSusChem,2011,vol.4,#6,p.785-791]

[15]Arthur,IsaacN.;Hennessy,JamesE.;Padmakshan,Dharshana;Stigers,DannonJ.;Lesturgez,Stéphanie;Fraser,SamuelA.;Liutkus,Mantas;Otting,Gottfried;Oakeshott,JohnG.;Easton,ChristopherJ.[Chemistry-AEuropeanJournal,2013,vol.19,#21,p.6824-6830]

[16]Ager,DavidJ.;Babler,Scott;Erickson,RobertA.;Froen,DianeE.;Kittleson,Jeannine;Pantaleone,DavidP.;Prakash,Indra;Zhi,Ben[OrganicProcessResearchandDevelopment,2004,vol.8,#1,p.72-85]

[17]CurrentPatentAssignee:PFIZERINC-US2561323,1948,A

1499-55-4    4652-65-7 

[1]NipponKagakuZasshi,1959,vol.80,p.492,494    Chem.Abstr.,1961,p.3452

[2]JournaloftheChemicalSociety,1950,p.3239,3243

67-56-1    4124-76-9    6384-08-3    1499-55-4 

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1953,vol.73,p.397    Chem.Abstr.,1954,p.2597

22102-66-5    1499-55-4    27167-50-6 

[1]Miroshnikov,A.I.etal.[JournalofgeneralchemistryoftheUSSR,1970,vol.40,#2,p.395-407][ZhurnalObshcheiKhimii,1970,vol.40,#2,p.429-443]

1499-55-4    4652-65-7    5563-61-1 

[1]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.451-454    ZhurnalObshcheiKhimii,1970,vol.40,p.487-491

[2]AustralianJournalofChemistry,1965,vol.18,p.1095-1103

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