cis-3-Hexen-1-yl Benzoate TCI B1039

Chemical Identity

CAS No.: 25152-85-6
PubChem: CID 5367706·SID 87563989
Formula: C13H16O2
Molecular weight: 204.26 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(Z)-hex-3-enyl] benzoate
SMILES: CC/C=C\CCOC(=O)C1=CC=CC=C1
InChIKey: BCOXBEHFBZOJJZ-ARJAWSKDSA-N

Rp 2.227.050,00

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Volume 25mL

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TCI B1039 25152-85-6 cis-3-Hexen-1-yl Benzoate is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it serves as a fundamental component in the creation of larger molecular structures. This compound is particularly valuable in research and development processes where precise chemical reactions are required. Its versatility makes it an essential tool for chemists working on various synthetic pathways.

The compound's unique molecular structure, featuring an ester group and a reactive hydrocarbon chain, contributes to its effectiveness in chemical reactions. Its volatility and solubility in organic solvents make it easy to handle and incorporate into different reaction conditions. These properties enhance its utility in both academic and industrial applications. The presence of the cis-3-hexen group adds specificity to its reactivity, allowing it to participate in targeted chemical transformations under controlled environments.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of new compounds with applications in pharmaceuticals, cosmetics, and industrial chemicals. It is also a valuable teaching tool, helping students understand the principles of organic synthesis and molecular reactivity. Its presence in educational and research settings underscores its importance in advancing chemical knowledge and innovation.

Related TCI products

Organic Synthesis: This compound is ideal for creating complex organic molecules due to its reactive ester group and hydrocarbon chain.
Esterification Reactions: Its ester functionality makes it suitable for reactions that require ester formation or modification.
Substitution Reactions: The cis-3-hexen group allows for specific substitution reactions, enhancing its utility in synthetic pathways.
Aromatic Compound Synthesis: It is used in the development of aromatic compounds, contributing to the creation of new chemical entities.
Educational Purposes: It serves as a practical teaching aid for students learning about organic synthesis and molecular reactivity.

Brand	TCI
CAS number	25152-85-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light and incompatible substances

This compound should be stored in a cool, dry place, away from direct light and incompatible materials. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its stability. Due to its volatility, it should be handled in a well-ventilated area or fume hood to minimize inhalation risks. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. It is important to avoid contact with skin and eyes, and to follow standard laboratory safety protocols to ensure safe usage and storage.

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