Ethyl 3-Phenylglycidate (cis- and trans- mixture) TCI E0798

Chemical Identity

Other names: 3-Phenylglycidic Acid Ethyl Ester (cis- and trans- mixture) · Ethyl 3-Phenyloxiranecarboxylate (cis- and trans- mixture)
CAS No.: 121-39-1
PubChem: CID 8469·SID 87560895
Formula: C11H12O3
Molecular weight: 192.21 g/mol
Purity: >90.0%(GC)
Storage: 0-10°C
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 3-phenyloxirane-2-carboxylate
SMILES: CCOC(=O)C1C(O1)C2=CC=CC=C2
InChIKey: GOMAKLPNAAZVCJ-UHFFFAOYSA-N
MDL: MDL00005123

Rp 477.750,00

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Ethyl 3-Phenylglycidate (cis- and trans- mixture) is a versatile organic compound widely used in laboratory settings for the synthesis of complex molecules. As a glycidate derivative, it serves as a building block in various organic reactions, including Diels-Alder and epoxide reactions. Its unique structure allows for multiple functional group transformations, making it an essential reagent in synthetic chemistry. This compound is particularly valuable for researchers aiming to develop new compounds with specific structural features.

The compound's reactivity and structural versatility make it a preferred choice in both academic and industrial research. It exhibits stability under controlled conditions but is sensitive to high temperatures and oxidative environments. These properties require careful handling to maintain its chemical integrity. Its distinct aroma also aids in its identification during laboratory work. Due to its broad applicability, Ethyl 3-Phenylglycidate is a go-to material for chemists working on aromatic and heterocyclic compound synthesis.

In Indonesian laboratories, Ethyl 3-Phenylglycidate is commonly used in organic chemistry research, especially in universities and research institutions. It plays a key role in teaching and experimental work, helping students and researchers understand reaction mechanisms and synthetic pathways. Its availability and reliability make it a staple in many chemical laboratories across the country.

Related TCI products

Organic synthesis of aromatic and heterocyclic compounds due to its reactive glycidate structure.
Facilitating Diels-Alder reactions by acting as a dienophile or diene depending on the reaction conditions.
Serving as a building block for the preparation of epoxide derivatives through ring-opening reactions.
Supporting the development of new chemical compounds in research and development settings.
Being used in educational laboratories to demonstrate reaction mechanisms and synthetic strategies.

Brand	TCI
CAS number	121-39-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Liquid or solid depending on the specific formulation
Storage	—

Ethyl 3-Phenylglycidate 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 sensitivity to oxidation, it should be stored in an inert atmosphere if possible. The compound should be handled with appropriate personal protective equipment to avoid skin contact and inhalation. Regular monitoring of storage conditions is essential to maintain its chemical stability and ensure safe usage in laboratory settings.

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