Julolidine TCI J0007

Chemical Identity

CAS No.: 479-59-4
PubChem: CID 68069·SID 87558509
Formula: C12H15N
Molecular weight: 173.25 g/mol
Purity: >97.0%(GC)(T)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8-triene
SMILES: C1CC2=C3C(=CC=C2)CCCN3C1
InChIKey: DZFWNZJKBJOGFQ-UHFFFAOYSA-N

Rp 1.961.400,00

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Julolidine, with CAS number 479-59-4, is a chemical compound widely used in various chemical reactions and the synthesis of complex molecules. As a heterocyclic compound, it features a core structure composed of two aromatic rings connected together, providing both stability and reactivity. This structural characteristic makes it a valuable building block in organic chemistry. Its ability to participate in multiple reaction types, such as substitution, reduction, and nucleophilic reactions, further enhances its utility in synthetic pathways.

Julolidine is preferred due to its chemical properties, including resistance to oxidation and the ability to form bonds with various functional groups. These characteristics make it a versatile reagent in the synthesis of heterocyclic compounds, such as indole derivatives and pyrrolidin derivatives. Its relatively low reactivity also ensures safety during controlled laboratory conditions, making it a reliable choice for researchers. The compound’s stability and functional versatility contribute to its widespread use in both academic and industrial settings.

In Indonesian laboratories, julolidine is commonly used in organic chemistry research, particularly in the development of new compounds with biological activity. It serves as a foundational material for synthesis experiments and characterization studies. Many research institutions and universities rely on julolidine as a key reagent for exploring molecular structures and functional group modifications. Its consistent performance and predictable behavior make it an essential component in laboratory workflows.

Related TCI products

Organic synthesis experiments benefit from julolidine's ability to participate in multiple reaction types, making it ideal for creating complex molecular structures.
Drug development research utilizes julolidine due to its role in synthesizing compounds with potential pharmaceutical applications.
Heterocyclic compound characterization relies on julolidine's stable structure, allowing for accurate analysis of molecular properties.
Academic research projects use julolidine as a foundational reagent for exploring new chemical pathways and molecular modifications.
Bioactive compound development leverages julolidine's reactivity to create molecules with targeted biological functions.

Brand	TCI
CAS number	479-59-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from light

Julolidine should be stored in a cool, dry place, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent contamination and moisture exposure. Due to its relatively low reactivity, it does not require special handling under normal laboratory conditions. However, it is advisable to work with it in a well-ventilated area to ensure safe handling. Proper labeling of containers is essential for identification and safety. Laboratory personnel should follow standard chemical handling protocols to minimize any potential risks associated with its use.

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