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4816-80-2,MFCD00020545
Catalog No.:AA006WW3

4816-80-2 | N-(P-Tolylsulphonyl)-l-glutamic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$29.00   $20.00
- +
5g
97%
in stock  
$45.00   $32.00
- +
25g
97%
in stock  
$95.00   $67.00
- +
100g
97%
in stock  
$245.00   $171.00
- +
500g
97%
in stock  
$992.00   $695.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA006WW3
Chemical Name:
N-(P-Tolylsulphonyl)-l-glutamic acid
CAS Number:
4816-80-2
Molecular Formula:
C12H15NO6S
Molecular Weight:
301.3156
MDL Number:
MFCD00020545
SMILES:
OC(=O)[C@@H](NS(=O)(=O)c1ccc(cc1)C)CCC(=O)O
Properties
Properties
 
BP:
534.2°C at 760 mmHg  
Form:
Solid  
MP:
122-137 °C  
Storage:
Keep in dry area;-20 ℃;  

Computed Properties
 
Complexity:
447  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
7  
XLogP3:
0.7  

Downstream Synthesis Route

[1]Srikanth;Debnath,Bikash;Jha,Tarun[BioorganicandMedicinalChemistry,2002,vol.10,#6,p.1841-1854]

[2]Swan;duVigneaud[JournaloftheAmericanChemicalSociety,1954,vol.76,p.3110,3112]

[1]Srikanth;Kumar;Ghosh,Balaram;Jha,Tarun[BioorganicandMedicinalChemistry,2002,vol.10,#7,p.2119-2131]

[2]Tanner,David;Somfai,Peter[Tetrahedron,1988,vol.44,#2,p.613-618]

[3]Rudinger[CollectionofCzechoslovakChemicalCommunications,1954,vol.19,p.365,373]Rudingeretal.[CollectionofCzechoslovakChemicalCommunications,1959,vol.24,p.2013,2014,2016]

[4]Harington;Moggridge[JournaloftheChemicalSociety,1940,p.706,712]

[5]Harington;Moggridge[JournaloftheChemicalSociety,1940,p.706,712]

[6]Paz,NievesR.;Rodríguez-Sosa,Dionisio;Valdés,Haydee;Marticorena,Ricardo;Melián,Daniel;Copano,M.Belén;González,ConcepciónC.;Herrera,AntonioJ.[OrganicLetters,2015,vol.17,#10,p.2370-2373]

[1]CurrentPatentAssignee:ACADEMYOFMILITARYMEDICALSCIENCES-US2011/306633,2011,A1Locationinpatent:Page/Pagecolumn4

[2]CurrentPatentAssignee:ACADEMYOFMILITARYMEDICALSCIENCES-EP2128137,2009,A1Locationinpatent:Page/Pagecolumn5

[3]CurrentPatentAssignee:HARMANFINOCHEMLTD-WO2016/103274,2016,A1Locationinpatent:Page/Pagecolumn10

[4]Srikanth;Debnath,Bikash;Jha,Tarun[BioorganicandMedicinalChemistry,2002,vol.10,#6,p.1841-1854]

[5]Srikanth;Kumar;Ghosh,Balaram;Jha,Tarun[BioorganicandMedicinalChemistry,2002,vol.10,#7,p.2119-2131]

[6]Yudasaka,Masaharu;Shimbo,Daisuke;Maruyama,Toshifumi;Tada,Norihiro;Itoh,Akichika[OrganicLetters,2019,vol.21,#4,p.1098-1102]

[7]Rudingeretal.[CollectionofCzechoslovakChemicalCommunications,1959,vol.24,p.2013,2014,2016]

[8]Hernandez,J.Nicolas;Ramirez,MiguelA.;Martin,VictorS.[JournalofOrganicChemistry,2003,vol.68,#3,p.743-746]

[9]CurrentPatentAssignee:TAIMEDBIOLOGICS,INC.-US2002/151546,2002,A1

4816-80-2    71-36-3   
<i>N</i>-(toluene-sulfonyl-(4))-L-glutamicaciddibutylester 

[1]McChesney;Swann[JournaloftheAmericanChemicalSociety,1937,vol.59,p.1116]

4816-80-2    149409-22-3   
C18H27N3O6S(2+)*2Cl(1-) 

[1]Nakonieczna,Lucja;Milewska,Maria;Kolasa,Teodozyj;Chimiak,Andrzej[Synthesis,1985,#10,p.929-931]

Literature

Title: Synthesis and evaluation of L-glutamic Acid analogs as potential anticancer agents.

Journal: Indian journal of pharmaceutical sciences 20080101

Title: The hydrogen-bonding network in (+)-N-tosyl-L-glutamic acid.

Journal: Acta crystallographica. Section C, Crystal structure communications 20050301

Title: Enantioselective chromenone benzoxazole receptor for glutamic acid and its derivatives.

Journal: The Journal of organic chemistry 20030919

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