Levofloxacin Q-Acid TCI L0238

Chemical Identity

CAS No.: 100986-89-8
PubChem: CID 688333·SID 160871226
Formula: C13H9F2NO4
Molecular weight: 281.21 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-6,7-difluoro-2-methyl-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid
SMILES: C[C@H]1COC2=C3N1C=C(C(=O)C3=CC(=C2F)F)C(=O)O
InChIKey: NVKWWNNJFKZNJO-YFKPBYRVSA-N

Rp 530.250,00

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Berat 1g 5g

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Levofloxacin Q-Acid (TCI L0238), with CAS number 100986-89-8, is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This material plays a crucial role in the laboratory by enabling the synthesis of complex organic compounds with precise stereochemistry. Its chiral nature allows for the creation of enantiomerically pure substances, which are essential in pharmaceutical and medicinal chemistry research. As a key building block, it supports the development of new therapeutic agents and advanced chemical structures.

The compound’s chiral structure and high purity make it a preferred choice for researchers seeking precise control over molecular configuration. Its stability and availability in pure form ensure reliable results in synthetic processes. These properties are particularly valuable in applications requiring high accuracy and reproducibility. The compound’s ability to participate in asymmetric reactions makes it an essential tool for scientists working on drug development and organic synthesis.

In Indonesian laboratories, Levofloxacin Q-Acid is commonly used in pharmaceutical and organic chemistry research. It is a fundamental component in the development of new medicinal compounds and is utilized by academic institutions and research centers. Its role in creating bioactive molecules supports advancements in medical science and chemical innovation within the region.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 5

Related TCI products

Asymmetric Synthesis: Levofloxacin Q-Acid is ideal for asymmetric synthesis due to its chiral structure, enabling the creation of enantiomerically pure compounds.
Pharmaceutical Research: Its use in drug development supports the synthesis of bioactive molecules with specific therapeutic applications.
Organic Chemistry Studies: The compound is widely used in organic synthesis to build complex molecular frameworks with precise stereochemistry.
Medicinal Chemistry Applications: It facilitates the design of new drugs by allowing controlled stereochemical outcomes in synthetic pathways.
Academic Research: Indonesian universities and research institutions rely on this compound for teaching and experimental studies in advanced chemistry.

Brand	TCI
CAS number	100986-89-8
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light

Levofloxacin Q-Acid should be stored in a cool, dry environment to maintain its stability and purity. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Proper disposal methods should be followed to ensure compliance with safety regulations. The compound is not inherently hazardous under normal storage conditions but requires careful handling to maintain its integrity and effectiveness in research applications.

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