Floctafenine

Floctafenine
LC Conditions
Column

Chirex (S)-VAL and (R)-NEA, LC Column 250 x 4.6 mm, Ea

Brand

Chirex

Part No

00G-3014-E0

Phase Name

3014 (S)-valine and (R)-1-(alpha-naphthyl)ethylamine

Elution Type

Isocratic

Mobile Phase

A: Hexane

B: Tetrahydrofuran

C: Ethanol

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

80

18

Flow Rate

1.00 mL/min

Temperature

22°C

Detection

UV-Vis Abs.-Variable Wave.(UV) @ (22°C)

Detection Info

Order Items Used in This Application

Chirex (S)-VAL and (R)-NEA, LC Column 250 x 4.6 mm, Ea
00G-3014-E0

Chirex (S)-VAL and (R)-NEA, LC Column 250 x 4.6 mm, Ea

View Product

  • 1. Floctafenine
  • 2. Floctafenine
-OEChem-06211003152D<br><br> 46 48  0     1  0  0  0  0  0999 V2000<br>    6.3349   -5.6723    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.3464   -4.6839    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.3466   -4.6608    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    2.3623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    4.3623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3301    5.3623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641    0.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -0.6377    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -3.6377    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641   -2.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981   -1.6377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641   -3.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3580   -3.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320   -0.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3580   -1.6031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320    0.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320   -2.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.2641   -3.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.2641   -2.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641    3.8623    0.0000 C   0  0  3  0  0  0  0  0  0  0  0  0<br>    5.4641    2.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3465   -4.6723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660   -0.6377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.7320   -3.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    1.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    1.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000   -0.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3301    4.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    0.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.1350   -0.3277    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3509   -0.9831    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1951   -1.8277    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.7998   -3.4706    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.7998   -1.8048    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.4641    4.4823    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.6762    2.2796    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.0747    2.9699    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660   -1.2577    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.1951   -3.4477    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.8660    1.9823    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.5422    3.7796    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.9407    4.4699    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.4631   -0.4477    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    1.4631    1.1723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5981    4.9823    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.8671    5.6723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1 22  1  0  0  0  0<br>  2 22  1  0  0  0  0<br>  3 22  1  0  0  0  0<br>  4 21  1  0  0  0  0<br>  4 26  1  0  0  0  0<br>  5 20  1  0  0  0  0<br>  5 45  1  0  0  0  0<br>  6 28  1  0  0  0  0<br>  6 46  1  0  0  0  0<br>  7 26  2  0  0  0  0<br>  8 11  1  0  0  0  0<br>  8 14  1  0  0  0  0<br>  8 30  1  0  0  0  0<br>  9 12  2  0  0  0  0<br>  9 24  1  0  0  0  0<br> 10 11  2  0  0  0  0<br> 10 12  1  0  0  0  0<br> 10 15  1  0  0  0  0<br> 11 17  1  0  0  0  0<br> 12 13  1  0  0  0  0<br> 13 18  2  0  0  0  0<br> 13 22  1  0  0  0  0<br> 14 16  1  0  0  0  0<br> 14 23  2  0  0  0  0<br> 15 19  2  0  0  0  0<br> 15 31  1  0  0  0  0<br> 16 25  2  0  0  0  0<br> 16 26  1  0  0  0  0<br> 17 24  2  0  0  0  0<br> 17 32  1  0  0  0  0<br> 18 19  1  0  0  0  0<br> 18 33  1  0  0  0  0<br> 19 34  1  0  0  0  0<br> 20 21  1  0  0  0  0<br> 20 28  1  0  0  0  0<br> 20 35  1  0  0  0  0<br> 21 36  1  0  0  0  0<br> 21 37  1  0  0  0  0<br> 23 27  1  0  0  0  0<br> 23 38  1  0  0  0  0<br> 24 39  1  0  0  0  0<br> 25 29  1  0  0  0  0<br> 25 40  1  0  0  0  0<br> 27 29  2  0  0  0  0<br> 27 43  1  0  0  0  0<br> 28 41  1  0  0  0  0<br> 28 42  1  0  0  0  0<br> 29 44  1  0  0  0  0<br>M  END
Compound Name

Floctafenine

CID

3360

Molecular Formula

C20H17F3N2O4

Molecular Weight

406

No. Hydrogen Bond Acceptors

9

No. Hydrogen Bond Donors

3

Similar Applications

No Similar applications found.