Phenyl Formate TCI P2770

Chemical Identity

CAS No.: 1864-94-4
PubChem: CID 74626·SID 468592713
Formula: C7H6O2
Molecular weight: 122.12 g/mol
Purity: >98.0%(GC)
Reference databases: Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: phenyl formate
SMILES: C1=CC=C(C=C1)OC=O
InChIKey: GEOWCLRLLWTHDN-UHFFFAOYSA-N

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Phenyl Formate (TCI P2770, CAS 1864-94-4) is an organic compound widely used in laboratory chemical reactions. As a key component in organic chemistry, it serves as a building block for the synthesis of aromatic compounds and esters. Its versatility makes it an essential reagent for researchers aiming to create complex molecular structures. This compound is commonly found in both academic and industrial laboratory settings, where it plays a crucial role in various synthetic pathways. Its chemical stability and reactivity with bases, acids, and alkali metals further enhance its utility in diverse chemical processes.

Phenyl Formate is preferred due to its stable chemical properties and favorable solubility in organic solvents. It has a relatively high boiling point, which makes it suitable for reactions requiring controlled thermal conditions. Its ability to participate in esterification and transesterification reactions makes it a reliable choice for organic synthesis. Additionally, it is non-toxic in small quantities, ensuring a safer working environment in the laboratory. These characteristics contribute to its widespread use in both research and educational settings.

In Indonesian laboratories, Phenyl Formate is frequently used in organic chemistry research, particularly in undergraduate and postgraduate studies. It is a common reagent in courses focused on synthetic organic chemistry and functional group transformations. Its availability and reliability make it a staple in both academic and industrial laboratory environments across Indonesia.

Related TCI products

Organic synthesis of aromatic compounds and esters due to its reactivity and structural versatility.
Esterification and transesterification reactions because of its ability to form ester linkages.
Teaching and research in undergraduate and postgraduate organic chemistry programs for practical demonstrations.
Development of complex molecular structures in pharmaceutical and materials science research.
Use in functional group transformations as a key intermediate in synthetic pathways.

Brand	TCI
CAS number	1864-94-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from direct sunlight

Phenyl Formate should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity with moisture, it should be kept in a desiccated environment. While it is generally considered safe in small quantities, standard laboratory safety protocols should be followed, including the use of personal protective equipment. Proper labeling and storage conditions are essential to ensure its effectiveness and safety in laboratory settings.

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