Home Nitro Compounds 2922-40-9
2922-40-9,MFCD00007384
Catalog No.:AA002XOZ

2922-40-9 | D,L-p-Nitrophenylalanine

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5g
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$13.00   $9.00
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25g
97%
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$48.00   $34.00
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100g
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$158.00   $111.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA002XOZ
Chemical Name:
D,L-p-Nitrophenylalanine
CAS Number:
2922-40-9
Molecular Formula:
C9H10N2O4
Molecular Weight:
210.1867
MDL Number:
MFCD00007384
SMILES:
OC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])N
Properties
Properties
 
BP:
414.1°C at 760 mmHg  
Form:
Solid  
MP:
236-237 °C (dec.)(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
243  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
1  
XLogP3:
-1.2  

Literature

Title: Comparison of fluorescence reagents for simultaneous determination of hydroxylated phenylalanine and nitrated tyrosine by high-performance liquid chromatography with fluorescence detection.

Journal: Biomedical chromatography : BMC 20120101

Title: Nitro-phenylalanine: a novel sensor for heat transfer in peptides.

Journal: The journal of physical chemistry. A 20110324

Title: Probing local environments with the infrared probe: L-4-nitrophenylalanine.

Journal: The journal of physical chemistry. B 20110317

Title: Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis.

Journal: PloS one 20100101

Title: 1H NMR determination of beta-N-methylamino-L-alanine (L-BMAA) in environmental and biological samples.

Journal: Toxicon : official journal of the International Society on Toxinology 20090401

Title: 2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.

Journal: Acta crystallographica. Section E, Structure reports online 20080801

Title: (S)-2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.

Journal: Acta crystallographica. Section E, Structure reports online 20080601

Title: Profiling of proteolytic enzymes in the gut of the tick Ixodes ricinus reveals an evolutionarily conserved network of aspartic and cysteine peptidases.

Journal: Parasites & vectors 20080101

Title: The genetic incorporation of a distance probe into proteins in Escherichia coli.

Journal: Journal of the American Chemical Society 20060412

Title: Efficient incorporation of a nonnatural amino acid into a protein in an insect cell-free translation system.

Journal: Nucleic acids symposium series (2004) 20060101

Title: Neighbouring group processes in the deamination of protonated phenylalanine derivatives.

Journal: Organic & biomolecular chemistry 20051021

Title: Synthesis of new bivalent peptides for applications in the Affinity Enhancement System.

Journal: Bioconjugate chemistry 20050101

Title: A novel competitive ELISA for both free and protein-bound nitrotyrosine.

Journal: Hybridoma and hybridomics 20031201

Title: Position-specific incorporation of a fluorophore-quencher pair into a single streptavidin through orthogonal four-base codon/anticodon pairs.

Journal: Journal of the American Chemical Society 20021211

Title: Influence of a ring substituent on the tendency to form H(2)O adducts to Ag(+) complexes with phenylalanine analogues in an ion trap mass spectrometer.

Journal: Journal of mass spectrometry : JMS 20020401

Title: 6-hydroxydopamine increases the hydroxylation and nitration of phenylalanine in vivo: implication of peroxynitrite formation.

Journal: Journal of neurochemistry 20010801

Title: Increase in fluorescence upon the hydrolysis of tyrosine peptides: application to proteinase assays.

Journal: Analytical biochemistry 19950501

Title: Sensitive, soluble chromogenic substrates for HIV-1 proteinase.

Journal: The Journal of biological chemistry 19900515

Title: Comparison of mu-, delta- and kappa-receptor binding sites through pharmacologic evaluation of p-nitrophenylalanine analogs of opioid peptides.

Journal: Life sciences 19830101

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Tags:2922-40-9 Molecular Formula|2922-40-9 MDL|2922-40-9 SMILES|2922-40-9 D,L-p-Nitrophenylalanine