Benzylideneaniline TCI B1034

Chemical Identity

CAS No.: 538-51-2
PubChem: CID 10858·SID 87563984
Formula: C13H11N
Molecular weight: 181.23 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N,1-diphenylmethanimine
SMILES: C1=CC=C(C=C1)C=NC2=CC=CC=C2
InChIKey: UVEWQKMPXAHFST-UHFFFAOYSA-N

Rp 1.961.400,00

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Benzylideneaniline (TCI B1034), with CAS number 538-51-2, is a chemical compound widely used in organic laboratory reactions. As a fundamental building block in the synthesis of complex molecules, it plays a crucial role in various chemical processes, including condensation, substitution, and cross-coupling reactions. Its versatility makes it a valuable tool for researchers aiming to modify molecular structures or develop new compounds. In Indonesian laboratories, this compound is frequently utilized for both academic and industrial research, supporting a wide range of chemical investigations.

Benzylideneaniline is known for its chemical stability and high reactivity, which make it an ideal substrate for reactions involving amino and aromatic groups. Its simple molecular structure allows for easy modification, enabling chemists to tailor its properties for specific applications. The compound’s solid form also facilitates handling and storage, making it a practical choice for laboratory use. These characteristics contribute to its popularity among Indonesian researchers working in organic chemistry.

In Indonesian laboratories, Benzylideneaniline is commonly used in pure and applied chemical research. It is a standard component in chemical laboratories, both for educational purposes and advanced research. Its availability and reliability ensure that it remains a key material for chemists seeking to explore new synthetic pathways and molecular transformations.

Related TCI products

Organic synthesis reactions benefit from Benzylideneaniline’s reactivity and structural flexibility, enabling the creation of complex molecules.
Cross-coupling reactions often utilize this compound due to its ability to participate in various reaction mechanisms, enhancing synthetic versatility.
Substitution reactions in aromatic systems are supported by its stable aromatic ring and reactive amino group, making it a valuable reagent.
Molecular modification studies rely on Benzylideneaniline’s simple structure, allowing for precise functional group transformations.
Educational laboratories use this compound to teach fundamental organic chemistry concepts and synthetic techniques.

Brand	TCI
CAS number	538-51-2
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

Benzylideneaniline should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation when working with the compound. It is advisable to store it away from incompatible substances to prevent any potential chemical interactions. Regular inspection of storage conditions ensures the compound remains in optimal condition for laboratory use.

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