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TCI

CAS 784-50-9

9-Fluorenone-2-carboxylic Acid TCI F0263

9-Fluorenone-2-carboxylic Acid TCI F0263

Chemical Identity

CAS No.
784-50-9
PubChem
CID 69913·SID 87570040
Formula
C14H8O3
Molecular weight
224.22 g/mol
Purity
>96.0%(HPLC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
9-oxofluorene-2-carboxylic acid
SMILES
C1=CC=C2C(=C1)C3=C(C2=O)C=C(C=C3)C(=O)O
InChIKey
BJCTXUUKONLPPK-UHFFFAOYSA-N
MDL
MDL00001156
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9-Fluorenone-2-carboxylic Acid is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a fundamental building block in chemical laboratories, particularly for the creation of both heterocyclic and non-heterocyclic compounds. This compound is commonly found in synthetic processes where functionalization and substitution reactions are required. Its versatility makes it an essential tool for researchers working on a variety of chemical transformations.

The compound is known for its stable molecular structure and favorable reactivity, which contribute to its effectiveness in various chemical applications. Its consistent chemical and physical properties ensure predictable outcomes in experimental settings, making it a reliable choice for laboratory use. The high chemical reactivity of 9-Fluorenone-2-carboxylic Acid allows it to participate in multiple reaction types, including esterification, hydrolysis, and substitution reactions. This makes it a valuable asset in both academic and industrial research environments.

In Indonesian laboratories, 9-Fluorenone-2-carboxylic Acid is frequently used in organic chemistry research, drug development, and the synthesis of new compounds. Its availability and high quality make it a preferred material for researchers seeking reliable and consistent results in their experiments. The compound’s role in advancing chemical synthesis and innovation is well recognized in the scientific community.

  • Organic synthesis reactions where functional group modification is required due to its reactivity and stability.
  • Drug development processes that involve the synthesis of complex heterocyclic compounds.
  • Research in chemical functionalization to create new derivatives with specific properties.
  • Industrial applications in the production of specialty chemicals and pharmaceutical intermediates.
  • Educational purposes in teaching advanced organic chemistry techniques and reaction mechanisms.

Brand TCI
CAS number 784-50-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

9-Fluorenone-2-carboxylic Acid should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a tightly sealed container to avoid moisture absorption and contamination. Proper labeling of containers is essential for safe handling and identification. The compound should be stored away from incompatible materials such as strong bases and reducing agents. Regular inspection of storage conditions ensures the integrity of the material. Always use appropriate personal protective equipment when handling this compound to ensure laboratory safety.

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