7-Nitro-9H-fluoren-2-ol | Solubility of Things

Identification

Molecular formula

C₁₃H₉NO₃

CAS number

36219-69-3

IUPAC name

7-nitro-9H-fluoren-2-ol

State

The compound is typically a crystalline solid at room temperature. Its yellow crystals are stable under normal conditions.

Melting point (Celsius)

180.00

Melting point (Kelvin)

453.15

Boiling point (Celsius)

522.10

Boiling point (Kelvin)

795.30

General information

Molecular weight

241.22g/mol

Molar mass

241.2100g/mol

Density

1.2760g/cm³

Appearence

The compound typically appears as a yellow crystalline solid. Its structure can form well-defined crystals, making it identifiable by its distinct yellow color and crystalline form.

Comment on solubility

Solubility of 7-nitro-9H-fluoren-2-ol

7-nitro-9H-fluoren-2-ol, with the chemical formula C₁₃H₉N₁O₂, exhibits interesting properties regarding its solubility. This compound is generally considered to be:

Moderately soluble in organic solvents: It can dissolve well in solvents such as ethanol, acetone, and chloroform.
Poorly soluble in water: Due to its hydrophobic fluorenyl group, 7-nitro-9H-fluoren-2-ol has limited solubility in aqueous solutions.

Factors influencing its solubility include:

Polarity of solvents: The polar nature of a solvent can significantly affect the dissolving process. Polar solvents tend to solubilize polar compounds better than non-polar solvents.
Temperature: Increased temperature can enhance solubility for many solids, allowing for greater interaction of solute and solvent molecules.

As a rule of thumb, one can say, "Like dissolves like." This means that substances with similar polarities will dissolve in each other more readily. Therefore, while 7-nitro-9H-fluoren-2-ol may not fare well in water, it thrives in organic environments, making it valuable in various chemical applications.

Interesting facts

Interesting Facts About 7-Nitro-9H-Fluoren-2-ol

7-Nitro-9H-fluoren-2-ol is a fascinating compound in the field of organic chemistry, particularly due to its intriguing structural features and applications. Below are some of the key points that make this compound noteworthy:

Unique Structure: The compound features a fluorenyl moiety, which contributes to its unique chemical properties. The presence of a nitro group enhances its reactivity, making it interesting for various chemical transformations.
Application in Organic Synthesis: 7-Nitro-9H-fluoren-2-ol plays a significant role in organic synthesis as an intermediate in the creation of more complex compounds. Its functional groups allow for selective reactions that chemists can harness.
Fluorescent Properties: Compounds with fluorenyl structures often exhibit interesting fluorescence characteristics, which can be instrumental in various applications, including biological imaging and sensor technology.
Potential in Material Science: Due to its solid framework, 7-nitro-9H-fluoren-2-ol is being explored for use in materials science, particularly in developing new polymers and organic light-emitting diodes (OLEDs).
Biochemical Significance: Certain derivatives of this compound are studied for their biological activities, which could lead to advancements in pharmaceuticals and therapeutic applications.

In summary, the exploration of 7-nitro-9H-fluoren-2-ol continues to inspire research across various domains, making it a valuable compound for both academic and practical applications. As noted by researchers, "the versatility of fluorenyl compounds opens new pathways for innovation in organic chemistry."

Synonyms

2-Hydroxy-7-nitrofluorene

6633-40-5

7-Nitro-9H-fluoren-2-ol

NSC 56690

CCRIS 8020

9H-Fluoren-2-ol, 7-nitro-

FLUOREN-2-OL, 7-NITRO-

BRN 2532810

DTXSID2074871

4-06-00-04847 (Beilstein Handbook Reference)

DTXCID9044794

7-Nitrofluoren-2-ol

7-Hydroxy-2-nitrofluorene

MLS002667838

NSC-56690

7-Nitro

HNF

NSC56690

CHEMBL165314

Y7H6768WBK

HMS3089B11

AKOS030239778

SMR001557595

DB-228121

Q27461148