ChemicalBook--->CAS DataBase List--->95713-52-3

95713-52-3

95713-52-3 Structure

95713-52-3 Structure
IdentificationBack Directory
[Name]

(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide
[CAS]

95713-52-3
[Synonyms]

FDAA
Marfey
Gold'
Comin'
S REAGENT
aninamide
MARFEY'
Belleau'
Togni&rsquo
Nα
FDNP-ALA-NH2
Lawesson&rsquo
FDNP-L-Ala-NH2
MARFEY'S REAGENT
L-Marfey's reagent
Nα-(2,4-Dinitro-5-fL
FATTYACIDMETHYLESTER
Marfey's reagent ,98%
FDAA, Marfeys reagent
FDNP-Ala-NH2( MARFEY'S REAGENT)
(3R,4S)-4-amino -3-hydroxypentanoic acid
N(ALPHA)-(2,4-DINITRO-5-FLUOROPHENYL)-L-
(2,4-Dinitro-5-fluorophenyl) L-Alaninamide
N(ALPHA)-(5)-2,4-DINITROPHENYL-L-ALANIMIDE
N2-(2,4-Dinitro-5-fluorophenyl)alaninamide
N2-(5-Fluoro-2,4-dinitrophenyl)alaninamide
Nα-(2,4-Dinitro-5-fluorophenyl)alaninamide
1-FLUORO-2,4-DINITROPHENYL-5-L-ALANINE AMIDE
nα-(2,4-dinitro-5-fluorophenyl)-l-alaninamide
Nα-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide
N2-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide
Nα-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alanine amide
NA-(2,4-DINITRO-5-FLUOROPHENYL)-L-*ALANI NAMIDE
Marfey's Reagent, 99%, for chiral derivatization
NALPHA-(5-FLUORO-2,4-DINITROPHENYL)-L-ALANINAMIDE
N-ALPHA-(2,4-DINITRO-5-FLUOROPHENYL)-L-ALANINAMIDE
(S)-2-(5-Fluoro-2,4-dinitrophenylaMino)propanaMide
N-ALPHA-(2,4-DINITRO-5-FLUOROPHENYL)-L-ALANINE AMIDE
(S)-2-[(5-Fluoro-2,4-dinitrophenyl)amino]propionamide
(2S)-2-[(5-Fluoro-2,4-dinitrophenyl)aMino]propanaMide
N-(2,4-Dinitro-5-fluorophenyl)-L-alaninaMide (powder)
PropanaMide,2-[(5-fluoro-2,4-dinitrophenyl)aMino]-, (2S)-
-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide
N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine (Ishikawa'
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alanine amide≥ 98% (HPLC)
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide USP/EP/BP
Nalpha-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide Marfey's Reagent
Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide,FDAA, Marfey’s reagent
FDAA, Marfeys reagent, Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide
N-a-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide[HPLClabellingreagentfore.e.determination)
Nα-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide[HPLCLabelingReagentfore.e.Determination]>
Nα-(5-Fluoro-2,4-dinitrophenyl)-L-alaninaMide [HPLC Labeling Reagent for e.e. DeterMination]
NALPHA-(2,4-DINITRO-5-FLUOROPHENYL)-L-ALANINAMIDE [HPLC LABELING REAGENT FOR E.E. DETERMINATION]
Nalpha-(5-Fluoro-2,4-dinitrophenyl)-L-alaninamide [HPLC Labeling Reagent for e.e. Determination]
[Molecular Formula]

C9H9FN4O5
[MDL Number]

MFCD00042049
[MOL File]

95713-52-3.mol
[Molecular Weight]

272.19
Chemical PropertiesBack Directory
[Melting point ]

229 °C
[Boiling point ]

544.5±50.0 °C(Predicted)
[density ]

1.592±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

acetone: 10 mg/mL, clear, yellow
[form ]

powder
[pka]

15.61±0.50(Predicted)
[color ]

yellow to orange
[Optical Rotation]

[α]20/D +56±2°, c = 1% in acetone
[BRN ]

6820069
[InChI]

InChI=1S/C9H9FN4O5/c1-4(9(11)15)12-6-2-5(10)7(13(16)17)3-8(6)14(18)19/h2-4,12H,1H3,(H2,11,15)/t4-/m0/s1
[InChIKey]

NEPLBHLFDJOJGP-BYPYZUCNSA-N
[SMILES]

C(N)(=O)[C@@H](NC1=CC(F)=C([N+]([O-])=O)C=C1[N+]([O-])=O)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

29242990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

Light yellow to yellow crystal or powder
[Uses]

(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide can be used for chiral amino acid analysis.
[General Description]

Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (FDAA) is a chiral derivatizing agent (CDA), has high enantioselectivity but low sensitivity as compared to other CDAs. It is generally used to assign the stereochemistry of amino acids in trace amounts.
[Biochem/physiol Actions]

N-α-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (FDAA) is a chiral derivatizing agent and is used routinely to improve the detection of underivatized amino acids in high performance liquid chromatography. Its usage is effective in separating stereoisomer.
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide(95713-52-3)1HNMR
(S)-2-(5-fluoro-2,4-dinitrophenylaMino)propanaMide(95713-52-3)IR
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