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CAS 68133-78-8

trans-2-Hexen-1-yl Phenylacetate TCI P1045

trans-2-Hexen-1-yl Phenylacetate TCI P1045

Chemical Identity

CAS No.
68133-78-8
Formula
C14H18O2
Molecular weight
218.29 g/mol
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
[(E)-hex-2-enyl] 2-phenylacetate
SMILES
CCC/C=C/COC(=O)CC1=CC=CC=C1
InChIKey
BYGAPGDXGHDYGP-XBXARRHUSA-N
PubChem
CID 5368236
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Trans-2-Hexen-1-yl Phenylacetate is a chemical compound widely used as a building block in the synthesis of complex molecules. It plays a crucial role in organic chemistry laboratories, where it serves as a versatile intermediate in the creation of various organic compounds. This compound is particularly valuable for its ability to participate in multiple chemical reactions, making it an essential tool for researchers and chemists. Its unique molecular structure, combining a hydrocarbon chain with a phenylacetate functional group, enables it to be a key player in synthetic pathways.

The compound's stability and controlled reactivity make it a preferred choice for laboratory applications. Its ability to undergo substitution and addition reactions allows for the development of a wide range of chemical structures. Additionally, its distinct aroma can serve as a visual indicator during certain reactions, aiding in the monitoring of chemical processes. These properties ensure that it remains a reliable and efficient material for use in both academic and industrial research settings.

In Indonesian laboratories, Trans-2-Hexen-1-yl Phenylacetate is commonly used in organic chemistry research, especially in the development of new compounds and pharmaceuticals. Its availability in high purity and ease of handling make it a popular choice among scientists. The compound's chemical stability also facilitates long-term storage and repeated use, enhancing its value in laboratory environments.

  • Organic synthesis is a primary application where this compound is used to build complex molecules due to its versatile functional groups and reactivity.
  • Pharmaceutical research benefits from its role in the development of new drug compounds, as it can be modified to create various bioactive molecules.
  • Chemical intermediates require this compound for the production of other chemicals, as it provides a stable base for further reactions.
  • Analytical chemistry uses it as a reference standard for identifying and quantifying similar compounds in complex mixtures.
  • Research and development in the chemical industry rely on its properties to create new materials and products with specific chemical characteristics.

Brand TCI
CAS number 68133-78-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

Trans-2-Hexen-1-yl Phenylacetate 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 exposure to moisture and air, which could affect its purity. Due to its potential reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. The compound is not flammable but should be kept away from incompatible substances. Regular monitoring of storage conditions ensures that the material remains in optimal condition for use in laboratory applications.

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