CAS 2922-40-9 | Phenylalanine, 4-nitro- | CAS Number 2922-40-9

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2922-40-9 | Phenylalanine, 4-nitro-

CAS No: 2922-40-9 Catalog No: AG002XRR MDL No:MFCD00007384

Product Description

Catalog Number:

AG002XRR

Chemical Name:

Phenylalanine, 4-nitro-

CAS Number:

2922-40-9

Molecular Formula:

C9H10N2O4

Molecular Weight:

210.1867

MDL Number:

MFCD00007384

IUPAC Name:

2-amino-3-(4-nitrophenyl)propanoic acid

InChI:

InChI=1S/C9H10N2O4/c10-8(9(12)13)5-6-1-3-7(4-2-6)11(14)15/h1-4,8H,5,10H2,(H,12,13)

InChI Key:

GTVVZTAFGPQSPC-UHFFFAOYSA-N

SMILES:

OC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])N

EC Number:

220-868-6

Properties

Complexity:

243

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

210.064g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

210.189g/mol

Monoisotopic Mass:

210.064g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

109A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

-1.2

Literature

Title	Journal
Comparison of fluorescence reagents for simultaneous determination of hydroxylated phenylalanine and nitrated tyrosine by high-performance liquid chromatography with fluorescence detection.	Biomedical chromatography : BMC 20120101
Nitro-phenylalanine: a novel sensor for heat transfer in peptides.	The journal of physical chemistry. A 20110324
Probing local environments with the infrared probe: L-4-nitrophenylalanine.	The journal of physical chemistry. B 20110317
Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis.	PloS one 20100101
1H NMR determination of beta-N-methylamino-L-alanine (L-BMAA) in environmental and biological samples.	Toxicon : official journal of the International Society on Toxinology 20090401
2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.	Acta crystallographica. Section E, Structure reports online 20080801
(S)-2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.	Acta crystallographica. Section E, Structure reports online 20080601
Profiling of proteolytic enzymes in the gut of the tick Ixodes ricinus reveals an evolutionarily conserved network of aspartic and cysteine peptidases.	Parasites & vectors 20080101
The genetic incorporation of a distance probe into proteins in Escherichia coli.	Journal of the American Chemical Society 20060412
Efficient incorporation of a nonnatural amino acid into a protein in an insect cell-free translation system.	Nucleic acids symposium series (2004) 20060101
Neighbouring group processes in the deamination of protonated phenylalanine derivatives.	Organic & biomolecular chemistry 20051021
Synthesis of new bivalent peptides for applications in the Affinity Enhancement System.	Bioconjugate chemistry 20050101
A novel competitive ELISA for both free and protein-bound nitrotyrosine.	Hybridoma and hybridomics 20031201
Position-specific incorporation of a fluorophore-quencher pair into a single streptavidin through orthogonal four-base codon/anticodon pairs.	Journal of the American Chemical Society 20021211
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 of mass spectrometry : JMS 20020401
6-hydroxydopamine increases the hydroxylation and nitration of phenylalanine in vivo: implication of peroxynitrite formation.	Journal of neurochemistry 20010801
Increase in fluorescence upon the hydrolysis of tyrosine peptides: application to proteinase assays.	Analytical biochemistry 19950501
Sensitive, soluble chromogenic substrates for HIV-1 proteinase.	The Journal of biological chemistry 19900515
Comparison of mu-, delta- and kappa-receptor binding sites through pharmacologic evaluation of p-nitrophenylalanine analogs of opioid peptides.	Life sciences 19830101