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Home Amines 1161-13-3
1161-13-3,MFCD00020418
Catalog No.:AA0035AO

1161-13-3 | (2S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanoic acid

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Purity
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5g
95%
in stock  
$11.00   $8.00
- +
25g
95%
in stock  
$16.00   $11.00
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100g
95%
in stock  
$51.00   $36.00
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500g
95%
in stock  
$110.00   $77.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0035AO
Chemical Name:
(2S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanoic acid
CAS Number:
1161-13-3
Molecular Formula:
C17H17NO4
Molecular Weight:
299.3212
MDL Number:
MFCD00020418
SMILES:
O=C(N[C@H](C(=O)O)Cc1ccccc1)OCc1ccccc1
Properties
Properties
 
BP:
511.5°C at 760 mmHg  
Form:
Solid  
MP:
85-88 °C  
Refractive Index:
5.3 ° (C=4, AcOH)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
360  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
7  
XLogP3:
2.1  

Upstream Synthesis Route

[1]JournaloftheChemicalSociety,FaradayTransactions1:PhysicalChemistryinCondensedPhases,1985,vol.81,p.2207-2214

[2]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1985,p.461-470

[3]JournaloftheChemicalSociety.Perkintransactions1,1966,vol.5,p.555-566

[1]TetrahedronLetters,1992,vol.33,#10,p.1347-1350

[2]Tetrahedron,2007,vol.63,#28,p.6577-6586

[3]JournalofOrganicChemistry,1976,vol.41,#20,p.3317-3321

[4]Synlett,2005,#18,p.2802-2804

[5]Synlett,2004,#3,p.477-480

[6]Synlett,2004,#3,p.477-480

[7]Synthesis,2002,#8,p.1121-1123

[8]BioorganicandMedicinalChemistryLetters,2000,vol.10,#11,p.1159-1162

[9]TetrahedronLetters,2000,vol.41,#32,p.6131-6135

[10]ChemicalandPharmaceuticalBulletin,1982,vol.30,#5,p.1921-1924

[11]TetrahedronLetters,1992,vol.33,#30,p.4257-4260

[12]Synlett,2013,vol.24,#6,p.747-751

[13]BioorganicandMedicinalChemistry,2013,vol.21,#17,p.5407-5413

[14]Patent:WO2015/95227,2015,A2,

[15]OrganicandBiomolecularChemistry,2015,vol.13,#42,p.10456-10460

[16]Patent:US2008/139556,2008,A1,

[1]Patent:US5206343,1993,A,

[1]BioorganicandMedicinalChemistry,2013,vol.21,#4,p.1018-1029

[1]JournalofMedicinalChemistry,2011,vol.54,#13,p.4365-4377

[2]BioorganicandMedicinalChemistry,2013,vol.21,#4,p.1018-1029

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1968,vol.21,p.2612-2617

[1]JournalofOrganicChemistry,1962,vol.27,p.2091-2093

1161-13-3    17083-23-7   
CbzNH-(L)-Phe-(L)-Tyr(O<SUP>t</SUP>Bu)-O<SUP>t</SUP>Bu 

[1]JournaloftheAmericanChemicalSociety,1963,vol.85,p.201-207

[2]Patent:US2018/99934,2018,A1.Locationinpatent:Paragraph0250-0253

[1]AngewandteChemie,1984,vol.96,p.702-704

[1]BulletinoftheChemicalSocietyofJapan,1991,vol.64,p.1533-1541

Literature

Title: Mechanism of the binding of Z-L-tryptophan and Z-L-phenylalanine to thermolysin and stromelysin-1 in aqueous solutions.

Journal: Biochimica et biophysica acta 20120201

Title: Synthesis, characterization and antimicrobial activity of Co(II), Zn(II) and Cd(II) complexes with N-benzyloxycarbonyl-S-phenylalanine.

Journal: European journal of medicinal chemistry 20090401

Title: Purification and characterization of cysteine protease from germinating cotyledons of horse gram.

Journal: BMC biochemistry 20090101

Title: Enantioseparation on molecularly imprinted monoliths--preparation and adsorption isotherms.

Journal: Analytica chimica acta 20070515

Title: Solid-phase peptide synthesis by ion-paired alpha-chymotrypsin in nonaqueous media.

Journal: Biotechnology and bioengineering 20030330

Title: Anticoagulant activity of sulfonated polyrotaxanes as blood-compatible materials.

Journal: Journal of biomedical materials research 20020401

Title: Synthesis of the marine natural product barbamide.

Journal: Chemical communications (Cambridge, England) 20011007

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Tags:1161-13-3 Molecular Formula|1161-13-3 MDL|1161-13-3 SMILES|1161-13-3 (2S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanoic acid