3-Aminobenzamide TCI A0630

Chemical Identity

CAS No.: 3544-24-9
PubChem: CID 1645·SID 87562201
Formula: C7H8N2O
Molecular weight: 136.15 g/mol
Purity: >98.0%(T)(HPLC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-aminobenzamide
SMILES: C1=CC(=CC(=C1)N)C(=O)N
InChIKey: GSCPDZHWVNUUFI-UHFFFAOYSA-N

Rp 2.702.700,00

~~Rp 1.905.750,00~~ Rp 2.702.700,00

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3-Aminobenzamide is a chemical compound widely used as a foundational building block in the synthesis of complex organic compounds. Its versatility makes it a critical component in various chemical reactions, particularly in the formation of heterocyclic structures and amine derivatives. In the laboratory, it serves as an essential reagent due to its ability to interact with a wide range of functional groups. This reactivity and adaptability make it a preferred choice for researchers engaged in the development of new compounds.

The compound’s reactive nature and flexible structure enable it to participate in multiple types of chemical reactions, including condensation, substitution, and nucleophilic reactions. The presence of an amino group at the 3-position and a carboxylic acid group at the 1-position enhances its reactivity and functional versatility. These characteristics make it highly suitable for use in organic synthesis and experimental research. Additionally, its stability under certain conditions ensures ease of storage and handling in laboratory settings.

In Indonesian laboratories, 3-Aminobenzamide is extensively used in both pure and applied chemical research. It is commonly found in experiments aimed at creating new compounds and understanding chemical mechanisms. Its availability and reliability make it a go-to material for researchers working on diverse chemical projects.

Related TCI products

Organic synthesis: 3-Aminobenzamide is ideal for constructing complex molecules due to its reactive functional groups.
Heterocyclic compound development: Its structure supports the formation of nitrogen-containing rings, making it useful in pharmaceutical research.
Amino acid derivatives: The amino group allows for easy modification, facilitating the synthesis of various amine-based compounds.
Condensation reactions: The carboxylic acid group enables participation in condensation reactions, aiding in the formation of esters and amides.
Analytical chemistry: It serves as a reference standard for identifying and quantifying similar compounds in analytical procedures.

Brand	TCI
CAS number	3544-24-9
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 moisture and direct sunlight

3-Aminobenzamide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent moisture absorption, which could affect its reactivity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Storage should be away from incompatible substances to avoid any potential chemical reactions. In laboratory settings, it is important to follow standard safety protocols to ensure safe handling and usage. Proper labeling of containers is also essential to prevent accidental exposure and ensure safe access.

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