CAS 153-78-6

2-Aminofluorene

Description:

2-Aminofluorene is an organic compound characterized by its structure, which consists of a fluorene backbone with an amino group (-NH2) positioned at the second carbon. This compound is a polycyclic aromatic amine, known for its potential mutagenic and carcinogenic properties, particularly in biological systems. It appears as a yellow to orange crystalline solid and is sparingly soluble in water but more soluble in organic solvents such as ethanol and acetone. 2-Aminofluorene is often used in research settings, particularly in studies related to mutagenesis and the mechanisms of carcinogenesis. Its reactivity is influenced by the amino group, which can participate in various chemical reactions, including electrophilic substitution and coupling reactions. Due to its biological implications, handling 2-aminofluorene requires caution, and it is subject to regulations regarding its use in laboratories. Overall, 2-aminofluorene serves as an important compound in both synthetic organic chemistry and toxicological studies.

Formula: C₁₃H₁₁N

InChI: InChI=1S/C13H11N/c14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7,14H2

InChI key: InChIKey=CFRFHWQYWJMEJN-UHFFFAOYSA-N

SMILES: NC=1C=C2C(C=3C(C2)=CC=CC3)=CC1

Synonyms:

• 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

2-Aminofluorene

CAS: 153-78-6

Formula: C₁₃H₁₁N

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Orange to Green powder to crystal

Molecular weight: 181.24

Ref: 3B-A0621

2-Aminofluorene, 98%

CAS: 153-78-6

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: C₁₃H₁₁N

Purity: 98%

Color and Shape: White to cream to yellow to pale brown, Powder or crystalline powder

Molecular weight: 181.24

Ref: 02-B22769

9H-fluoren-2-amine

CAS: 153-78-6

Formula: C₁₃H₁₁N

Purity: 98%

Color and Shape: Solid

Molecular weight: 181.2331

Ref: IN-DA003GJE

2-Aminofluorene

CAS: 153-78-6

2-Aminofluorene

Purity: ≥98%

Molecular weight: 181.23g/mol

Ref: 54-BUP18226

2-Aminofluorene

CAS: 153-78-6

Formula: C₁₃H₁₁N

Molecular weight: 181.23

Ref: 7W-GX1017

2-Aminofluorene-9-13C

CAS: 153-78-6, 335081-08-8

Purity: 99 atom % 13C

Color and Shape: White Brown Solid.

Molecular weight: 182.25

Ref: 3U-C5021

2-Aminofluorene

CAS: 153-78-6

Purity: 99.0%

Color and Shape: Solid

Molecular weight: 181.23800659179688

Ref: 10-F019454

2-Aminofluorene

CAS: 153-78-6

2-Aminofluorene (2-Fluorenamine) is a biochemical.

Formula: C₁₃H₁₁N

Purity: 99.9%

Color and Shape: Light Yellow Crystalline

Molecular weight: 181.23

Ref: TM-T21285

2-Aminofluorene

CAS: 153-78-6

2-Aminofluorene

Purity: 99%

Molecular weight: 181.23g/mol

Ref: 54-OR322035

2-Aminofluorene

CAS: 153-78-6

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: C₁₃H₁₁N

Color and Shape: White Powder

Molecular weight: 181.23 g/mol

Ref: 3D-FA33811