CAS 153-78-6
:2-Aminofluorene
- 2-Amino-9H-Fluoren
- 2-Amino-9H-fluorene
- 2-Fluorenamine
- 2-Fluoreneamine
- 2-Fluorenylamine
- 9H-Fluoren-2-amine
- 9H-fluoren-1-amine
- Fluoren-2-Am
- Fluoren-2-Amine
- Fluoren-2-Ilamina
- Fluoren-2-Ylamine
- Fluoren-2-ylamin
- Fluorene, 2-Amino-
- Fluorene-2-Ylamine
- N-2-Fluorenylamine
- Nsc 12274
- Nsc 26328
- Vedi altri sinonimi
2-Aminofluorene
CAS:Formula:C13H11NPurezza:>98.0%(T)(HPLC)Colore e forma:White to Orange to Green powder to crystalPeso molecolare:181.242-Aminofluorene, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C13H11NPurezza:98%Colore e forma:White to cream to yellow to pale brown, Powder or crystalline powderPeso molecolare:181.242-Aminofluorene-9-13C
CAS:Purezza:99 atom % 13CColore e forma:White Brown Solid.Peso molecolare:182.252-Aminofluorene
CAS:2-Aminofluorene (2-Fluorenamine) is a biochemical.Formula:C13H11NPurezza:99.9%Colore e forma:Light Yellow CrystallinePeso molecolare:181.232-Aminofluorene
CAS:2-Aminofluorene is a nucleoside phosphonate that is used in the study of DNA duplexes and as a possible anticancer drug. It has shown to be toxic to cells, such as HL-60 cells, by lysing them. This compound has also been shown to have an effect on polymerase chain reaction (PCR) by inhibiting the enzyme activity of DNA polymerase, which led to the cell lysis. 2-Aminofluorene binds to DNA at the minor groove of the double helix and prevents the formation of hydrogen bonds between complementary bases, causing steric hindrance that leads to cell death. 2-Aminofluorene shows conformational properties that are similar to acyclic nucleosides, such as cytidine and adenosine.
Formula:C13H11NColore e forma:White PowderPeso molecolare:181.23 g/mol








