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Chemical Structure| 19883-78-4 Chemical Structure| 19883-78-4
Chemical Structure| 19883-78-4

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H-Phe(2-F)-OH is a fluorinated phenylalanine derivative mainly used in drug design and research.

Synonyms: 2-Fluoro-L-phenylalanine

4.5 *For Research Use Only !

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Product Details of H-Phe(2-F)-OH

CAS No. :19883-78-4
Formula : C9H10FNO2
M.W : 183.18
SMILES Code : [H][C@](N)(CC1=C(F)C=CC=C1)C(O)=O
Synonyms :
2-Fluoro-L-phenylalanine
MDL No. :MFCD00066448

Safety of H-Phe(2-F)-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of H-Phe(2-F)-OH

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 19883-78-4 ]

[ 19883-78-4 ] Synthesis Path-Downstream   1~9

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  • [ 58632-95-4 ]
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  • [ 114873-00-6 ]
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  • [ 24424-99-5 ]
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YieldReaction ConditionsOperation in experiment
85% With sodium hydroxide; In water; EXAMPLE 39 N-Z-N'-{N-(2S,3S)-trans-ethoxycarbonyloxirane-2-carbonyl]-o-fluoro-L-phenylalanyl}-1,4-diaminobutane In a mixture of dioxanes (10 ml) and water (5 ml), o-fluoro-L-phenylalanine (1.00 g, manufactured by Wako Pure Chemical Industries, Ltd.) was dissolved. To the solution were added, while stirring under ice-cooling conditions, a 1N aqueous solution of sodium hydroxide (5.46 ml) and di-tert-butyl dicarbonate (1.38 ml), followed by stirring for one hour at room temperature. The reaction mixture was concentrated, then the pH was adjusted to 2.5, followed by extraction with ethyl acetate (100 ml *3). The ethyl acetate layer was washed with water and a saturated saline, dried over anhydrous sodium sulfate. After concentration, the concentrate was crystallized from ethyl acetate--petroleum ether to yield N-Boc-o-fluoro-L-phenylalanine (1.32 g) as colorless crystals (yield 85%).
  • 4
  • [ 18944-77-9 ]
  • [ 19883-78-4 ]
YieldReaction ConditionsOperation in experiment
With ammonium carbamate; at 30℃; for 17h;pH 9.1; General procedure: The reaction mixtures containing substituted (E)-cinnamic acids(2a-s, 5 mM) in NH2CO2NH4 (3 M, pH 9.1) supplemented with PzaPAL(50 Xg mL-1) or in NH3 (6 M, pH 10) supplemented with PcPAL (50 XgmL-1) were incubated at 30 C. Samples (50 XL) taken at different timepoints (17, 40, 64, and 168 h) from the reaction mixtures were quenchedby adding an equal volume of MeOH, vortexed and centrifuged(13,000 rpm, 2 min). The supernatant was transferred to a 0.22 Xmfilter and used directly for HPLC analysis to determine conversion andee values.
  • 5
  • 2-Amino-3-(2-fluoro-phenyl)-propionic acid isobutyl ester; hydrochloride [ No CAS ]
  • [ 19883-78-4 ]
  • [ 97731-02-7 ]
  • 7
  • C9H8FNO2 [ No CAS ]
  • [ 19883-78-4 ]
  • [ 97731-02-7 ]
  • 8
  • [ 451-69-4 ]
  • [ 151911-32-9 ]
  • [ 19883-78-4 ]
  • [ 97731-02-7 ]
  • (R)-β-amino-β-(2-fluorophenyl)propionic acid [ No CAS ]
  • 9
  • [ 451-69-4 ]
  • [ 19883-78-4 ]
  • [ 97731-02-7 ]
 

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