cis-3-Hexen-1-yl Tiglate TCI T0934

Chemical Identity

CAS No.: 67883-79-8
PubChem: CID 15461361·SID 87576752
Formula: C11H18O2
Molecular weight: 182.26 g/mol
Purity: >97.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(Z)-hex-3-enyl] (E)-2-methylbut-2-enoate
SMILES: CC/C=C\CCOC(=O)/C(=C/C)/C
InChIKey: JNWQKXUWZWKUAY-JQEGGOPCSA-N

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Volume 25mL

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TCI T0934 67883-79-8 cis-3-Hexen-1-yl Tiglate is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a building block in organic chemistry, it serves as a fundamental component in various chemical reactions. This compound is particularly valuable for its reactivity and compatibility with multiple functional groups, making it a versatile tool for chemists. Its role in laboratory research is critical, especially in the development of new compounds and the exploration of chemical reactivity patterns.

The compound’s molecular structure, featuring a tiglate group, contributes to its reactivity and ability to participate in esterification and substitution reactions. These properties make it a preferred choice for researchers aiming to create aromatic and aliphatic compounds. Its chemical stability under controlled conditions further enhances its usability, allowing for efficient handling and storage. This stability ensures that the compound remains effective throughout the synthesis process, supporting consistent results in experimental work.

In Indonesian laboratories, TCI T0934 67883-79-8 cis-3-Hexen-1-yl Tiglate is commonly used in organic chemistry research, particularly in academic and research institutions. Its availability and effectiveness in complex synthesis processes make it a favored material among scientists. The compound supports a wide range of applications, from basic research to advanced chemical development, making it an essential part of the laboratory toolkit.

Related TCI products

Synthesis of complex ester compounds for structural studies due to its reactivity and compatibility with various functional groups.
Organic chemistry research in academic institutions for the development of new chemical structures and molecular frameworks.
Esterification reactions in laboratory settings where the compound serves as a key reagent for forming ester bonds.
Substitution reactions in synthetic pathways, where the compound’s functional groups enable targeted chemical modifications.
Development of aromatic and aliphatic compounds, leveraging the compound’s structural versatility and chemical stability.

Brand	TCI
CAS number	67883-79-8
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 moisture

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. In laboratory settings, proper ventilation should be ensured when handling the compound to minimize inhalation risks. Avoid contact with incompatible materials, such as strong bases or oxidizing agents, to prevent unwanted reactions. Always use appropriate personal protective equipment, including gloves and safety goggles, when working with this compound to ensure safe handling and storage practices.

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