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CAS 4403-69-4

2-Aminobenzylamine TCI A1435

2-Aminobenzylamine TCI A1435

Chemical Identity

CAS No.
4403-69-4
PubChem
CID 178096·SID 87562889
Formula
C7H10N2
Molecular weight
122.17 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(aminomethyl)aniline
SMILES
C1=CC=C(C(=C1)CN)N
InChIKey
GVOYKJPMUUJXBS-UHFFFAOYSA-N
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2-Aminobenzylamine (CAS No. 4403-69-4) is a chemical compound widely used as a foundational building block in organic synthesis. It plays a crucial role in laboratories by enabling the creation of complex organic molecules through its reactivity and versatility. This compound is commonly employed in various chemical reactions, particularly in the formation of heterocyclic compounds and more intricate carbon chains. Its presence in synthetic pathways makes it an essential reagent for researchers working in organic chemistry and related fields.

The compound's simple molecular structure and high reactivity make it a preferred choice for synthetic chemists. It readily forms bonds with a variety of functional groups, allowing for the modification of carbon chains and the incorporation of amino groups. These characteristics make it ideal for applications requiring functional group manipulation or the development of bioactive molecules. Its ability to participate in substitution, coupling, and bonding reactions further enhances its utility in laboratory settings.

In Indonesian laboratories, 2-Aminobenzylamine is frequently utilized in organic chemistry, pharmacology, and the synthesis of bioactive compounds. It is particularly relevant for research involving drug development, industrial chemical formulations, and the modification of compounds for specific applications. Its widespread use underscores its importance in both academic and industrial research environments.

  • Organic synthesis for creating complex molecules due to its reactivity and versatility in forming new bonds.
  • Pharmacological research to develop bioactive compounds and pharmaceuticals through functional group modification.
  • Heterocyclic compound synthesis as a key intermediate in the formation of ring structures with nitrogen atoms.
  • Industrial chemical formulation for the production of specialty chemicals and intermediates.
  • Bioactive compound modification to tailor molecular structures for specific biological activities and applications.

Brand TCI
CAS number 4403-69-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply options
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible materials

2-Aminobenzylamine should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent exposure to air and moisture. Due to its reactivity, it should be stored separately from strong oxidizing agents and acids. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper ventilation is essential to minimize inhalation risks. Regular monitoring of storage conditions ensures the compound remains stable and safe for use in research applications.

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