Antibacterial compounds using Gemini 5u C6-Phenyl

Antibacterial compounds using Gemini 5u C6-Phenyl
LC Conditions
Column

Gemini 5 µm C6-Phenyl 110 Å, LC Column 150 x 4.6 mm, Ea

Brand

Gemini

Part No

00F-4444-E0

Phase Name

C6-Phenyl

Elution Type

Isocratic

Mobile Phase

A: 20mM Potassium Phosphate pH 2.5

B: Acetonitrile

Gradient Profile

Step No.

Time(min)

%A

%B

1

0

70

30

Flow Rate

1.00 mL/min

Temperature

22°C

Detection

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

Detection Info
Sample Notes

SecurityGuard™ Guard Cartridge System extends column lifetime. - SecurityGuard Cartridges, Gemini C6-Phenyl 4 x 3.0mm, 10/Pk Part No.: AJ0-7915 - Holder Part No.: KJ0-4282

Order Items Used in This Application

Gemini 5 µm C6-Phenyl 110 Å, LC Column 150 x 4.6 mm, Ea
00F-4444-E0

Gemini 5 µm C6-Phenyl 110 Å, LC Column 150 x 4.6 mm, Ea

View Product

  • 1. Furazolidone
  • 2. Nalidixic acid
  • 3. Sulfamethoxazole
-OEChem-04281016552D<br><br> 23 24  0     0  0  0  0  0  0999 V2000<br>    9.2665   -0.5210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.5032   -0.2088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.6787   -1.3300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.0000    0.7391    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0<br>    2.5352   -0.9082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.9575    0.4301    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    7.0064    0.7391    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0<br>    2.7431    0.0699    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0<br>    8.7665    1.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    9.5755    0.4301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    8.2665   -0.5210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.3122    0.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.2633    0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.0032    1.3300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.6942    0.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    4.0032    1.3300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0<br>    9.1814    1.4786    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    8.3516    1.4786    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>   10.1419    0.1779    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    9.8855    0.9670    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    6.3922   -0.5365    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    5.3676    1.8316    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>    3.6388    1.8316    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0<br>  1 10  1  0  0  0  0<br>  1 11  1  0  0  0  0<br>  2 12  1  0  0  0  0<br>  2 15  1  0  0  0  0<br>  3 11  2  0  0  0  0<br>  4  8  1  0  0  0  0<br>  5  8  2  0  0  0  0<br>  6  7  1  0  0  0  0<br>  6  9  1  0  0  0  0<br>  6 11  1  0  0  0  0<br>  7 13  2  0  0  0  0<br>  8 15  1  0  0  0  0<br>  9 10  1  0  0  0  0<br>  9 17  1  0  0  0  0<br>  9 18  1  0  0  0  0<br> 10 19  1  0  0  0  0<br> 10 20  1  0  0  0  0<br> 12 13  1  0  0  0  0<br> 12 14  2  0  0  0  0<br> 13 21  1  0  0  0  0<br> 14 16  1  0  0  0  0<br> 14 22  1  0  0  0  0<br> 15 16  2  0  0  0  0<br> 16 23  1  0  0  0  0<br>M  CHG  2   4  -1   8   1<br>M  END
Compound Name

Furazolidone

CID

5323714

Molecular Formula

C8H7N3O5

Molecular Weight

225

No. Hydrogen Bond Acceptors

6

Similar Applications

No Similar applications found.