Allyl Benzoate TCI B2041

Chemical Identity

CAS No.: 583-04-0
PubChem: CID 11406·SID 87564918
Formula: C10H10O2
Molecular weight: 162.18 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: prop-2-enyl benzoate
SMILES: C=CCOC(=O)C1=CC=CC=C1
InChIKey: LYJHVEDILOKZCG-UHFFFAOYSA-N

Rp 2.702.700,00

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

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Berat 25g

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Allyl Benzoate is a chemical compound widely utilized in laboratory settings for the synthesis of complex molecules. It serves as a key building block in organic chemistry, particularly in reactions that require functional group manipulation. The compound consists of a benzoate group attached to an allyl chain, making it a versatile reagent in the creation of aromatic and heterocyclic compounds. Its unique structure allows it to participate in various chemical transformations, including esterification, substitution, and cross-coupling reactions.

Allyl Benzoate is valued for its chemical stability under controlled conditions, although it is sensitive to oxidation and UV light exposure. This sensitivity necessitates careful handling and storage to maintain its integrity. The compound is typically a liquid with a distinct aroma and a relatively high boiling point. Its reactivity and ability to remain stable during chemical processes make it a preferred choice for researchers aiming to synthesize new compounds without significant degradation.

In Indonesian laboratories, Allyl Benzoate is commonly used in organic chemistry research, especially in academic institutions and research centers focused on the development of new chemical compounds. It is also found in pharmaceutical and industrial laboratories, where it plays a role in the formulation of pharmaceutical products and the production of chemical intermediates. Its application spans across multiple scientific disciplines, making it an essential reagent in modern chemical synthesis.

TCI brochures (PDF)

Biomaterials Research Reagents 2025-02-19 · p. 16
Monomers 2025-05-28 · p. 17

Related TCI products

Organic synthesis applications benefit from Allyl Benzoate's ability to participate in esterification and substitution reactions, facilitating the creation of complex aromatic compounds.
Cross-coupling reactions often utilize Allyl Benzoate due to its reactivity and compatibility with various catalysts, enhancing the efficiency of synthetic pathways.
Pharmaceutical research leverages Allyl Benzoate for the development of new drug compounds, as it can be modified to produce bioactive molecules.
Industrial chemical production uses Allyl Benzoate as a building block for the synthesis of specialty chemicals and intermediate products.
Research in heterocyclic chemistry benefits from Allyl Benzoate's structural versatility, allowing for the design of diverse molecular frameworks.

Brand	TCI
CAS number	583-04-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dark place away from oxidizing agents and UV light

Allyl Benzoate should be stored in a cool, dark environment to prevent degradation due to oxidation and UV exposure. It is recommended to use airtight containers made of glass or polyethylene to minimize contact with air and moisture. The compound is sensitive to light, so storage in a sealed, opaque container is essential. In laboratory settings, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and goggles, should be worn. Avoid prolonged exposure to heat and direct sunlight to maintain its chemical integrity and ensure safe usage.

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