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TCI

CAS 57042-08-7

Diethyl trans-3-Hexenedioate TCI B1592

Diethyl trans-3-Hexenedioate TCI B1592

Chemical Identity

CAS No.
57042-08-7
PubChem
CID 6148048·SID 87564495
Formula
C10H16O4
Molecular weight
200.23 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
diethyl (E)-hex-3-enedioate
SMILES
CCOC(=O)C/C=C/CC(=O)OCC
InChIKey
YIDKJPKYCLMJQW-AATRIKPKSA-N
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Diethyl trans-3-Hexenedioate is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it plays a crucial role in the development of both heterocyclic and non-heterocyclic compounds. Its unique molecular structure, featuring two ethyl groups attached to a trans-3-hexenedioate backbone, makes it a versatile reagent in various synthetic pathways. This compound is particularly valued for its ability to participate in key reactions such as Diels-Alder and esterification, making it indispensable in advanced chemical research.

The compound exhibits chemical stability under controlled conditions, although it is sensitive to moisture and air exposure. These properties make it suitable for use in high-temperature reactions or vacuum conditions. Its high boiling point ensures that it remains stable during prolonged heating processes, which is essential for many synthetic procedures. Additionally, its chemical inertness in specific environments allows it to be a reliable component in multi-step syntheses without unwanted side reactions.

In Indonesian laboratories, Diethyl trans-3-Hexenedioate is commonly used in organic chemistry research, especially in the synthesis of complex compounds and drug development. It is a preferred choice for researchers due to its reliability, versatility, and compatibility with a wide range of chemical reactions. Its application in both academic and industrial research settings underscores its importance in the chemical sciences.

  • Organic synthesis of complex molecules due to its reactivity and structural versatility.
  • Development of heterocyclic and non-heterocyclic compounds in pharmaceutical research.
  • Facilitation of Diels-Alder reactions for the formation of six-membered ring structures.
  • Use in esterification reactions to create ester derivatives with specific functional groups.
  • Support for high-temperature and vacuum-based synthetic processes due to its thermal stability.

Brand TCI
CAS number 57042-08-7
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 moisture and air exposure

Diethyl trans-3-Hexenedioate should be stored in a cool, dry environment to prevent degradation. It is recommended to use sealed containers to minimize exposure to moisture and air, which can affect its stability. The compound should be kept away from heat sources and direct sunlight to maintain its chemical integrity. In laboratory settings, it is advisable to handle the material in a well-ventilated area to ensure safety. Proper labeling of storage containers is essential for identification and safe handling. Regular monitoring of storage conditions ensures that the compound remains suitable for use in chemical reactions.

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