3-Bromo-4-nitrobenzoic Acid TCI B4786

Chemical Identity

CAS No.: 101420-81-9
PubChem: CID 16218087·SID 354334134
Formula: C7H4BrNO4
Molecular weight: 246.01 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromo-4-nitrobenzoic acid
SMILES: C1=CC(=C(C=C1C(=O)O)Br)[N+](=O)[O-]
InChIKey: KKPPNEJUUOQRLE-UHFFFAOYSA-N

Rp 1.670.550,00

~~Rp 1.183.350,00~~ Rp 1.670.550,00

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3-Bromo-4-nitrobenzoic Acid is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. This compound serves as a key building block in the development of complex organic molecules, enabling chemists to create a variety of functional groups and molecular structures. Its presence in chemical reactions allows for the modification of aromatic rings through substitution and functionalization, making it an essential tool in synthetic chemistry. Due to its reactivity and structural complexity, it is frequently employed in both academic and industrial research environments.

The compound’s unique combination of bromo, nitro, and carboxylic acid functional groups contributes to its high reactivity and selectivity in chemical reactions. These properties make it a preferred choice for chemists aiming to achieve specific reaction outcomes. The stability of the molecule under controlled conditions ensures consistent results, which is crucial for reproducibility in laboratory experiments. Additionally, its compatibility with various reaction conditions and reagents enhances its utility across different synthetic pathways.

In Indonesian laboratories, 3-Bromo-4-nitrobenzoic Acid is commonly used in organic chemistry research, particularly in higher education and industrial applications. It plays a vital role in teaching and research, helping students and scientists understand reaction mechanisms and molecular behavior. Its use in chemical analysis and synthetic processes supports the development of new compounds with potential applications in pharmaceuticals and materials science.

Related TCI products

Organic synthesis for the creation of complex molecules and functional groups in pharmaceutical research.
Nitration and electrophilic substitution reactions due to its reactive bromo and nitro groups.
Teaching and research in Indonesian universities for understanding aromatic ring modifications.
Industrial chemical production where precise molecular structures are required for product development.
Analytical chemistry experiments to study reaction mechanisms and molecular behavior under controlled conditions.

Brand	TCI
CAS number	101420-81-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	As listed on product page
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

3-Bromo-4-nitrobenzoic Acid should be stored in a cool, dry place away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound to minimize inhalation risks. Storage conditions should be controlled to avoid any potential degradation of the compound, ensuring its effectiveness in chemical reactions and research applications.

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