CAS 1214-32-0

7-Nitro-9H-fluoren-2-amine

Description:

7-Nitro-9H-fluoren-2-amine, with the CAS number 1214-32-0, is an organic compound characterized by its fluorenyl structure, which consists of a fused ring system. The presence of a nitro group (-NO2) at the 7-position and an amino group (-NH2) at the 2-position of the fluorenyl framework contributes to its chemical reactivity and potential applications. This compound is typically a yellow to orange crystalline solid, indicating its potential for colorimetric applications. It is soluble in organic solvents but may have limited solubility in water. The nitro group can participate in electrophilic substitution reactions, while the amino group can act as a nucleophile, making this compound useful in various synthetic pathways. Additionally, 7-Nitro-9H-fluoren-2-amine has been studied for its biological activities, including potential roles in pharmaceuticals and as a dye. Safety data should be consulted, as nitro compounds can be hazardous and may require careful handling and storage.

Formula: C₁₃H₁₀N₂O₂

InChI: InChI=1S/C13H10N2O2/c14-10-1-3-12-8(6-10)5-9-7-11(15(16)17)2-4-13(9)12/h1-4,6-7H,5,14H2

InChI key: InChIKey=IJMROTSXJSMTPW-UHFFFAOYSA-N

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

Synonyms:

• 2-Amino-7-Nitrofluoroene
• 7-Nitro-9 H-Fluoren-2-Ylamine
• 7-Nitro-Fluoren-2-Amin
• 7-Nitro-fluoren-2-amine
• 7-nitro-9H-fluoren-2-amine
• 9H-Fluoren-2-amine, 7-nitro-
• Fluoren-2-amine, 7-nitro-
• N-Ace
• Nsc 12278
• 2-Amino-7-nitrofluorene

2-Amino-7-nitrofluorene

Controlled Product

CAS: 1214-32-0

Applications A mutagenic aromatic nitro compound.
References Kier, L., et al.: Pharmacol. Res., 7, 801 (1990), Benigni, R., et al.: J. Med. Chem., 38, 629 (1995), Benigni, R., et al.: Mutat. Res., 371, 29 (1996),

Formula: C₁₃H₁₀N₂O₂

Color and Shape: Neat

Molecular weight: 226.23

Ref: TR-A618405