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CAS 29823-18-5

Ethyl 7-Bromoheptanoate TCI B1880

Ethyl 7-Bromoheptanoate TCI B1880

Chemical Identity

CAS No.
29823-18-5
PubChem
CID 122490·SID 87564768
Formula
C9H17BrO2
Molecular weight
237.13 g/mol
Purity
>97.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ethyl 7-bromoheptanoate
SMILES
CCOC(=O)CCCCCCBr
InChIKey
OOBFNDGMAGSNKA-UHFFFAOYSA-N
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Ethyl 7-Bromoheptanoate is a chemical compound widely used in organic reactions for the synthesis of complex molecules. As a building block in chemical laboratories, it serves as a versatile intermediate that can be modified through substitution or other reaction mechanisms. This compound is commonly found in synthetic processes where the extension of carbon chains is required. Its role in laboratory settings is critical for the development of new compounds with specific functional groups.

The compound's molecular structure is stable, and it exhibits good reactivity, making it an ideal choice for reactions involving bromo substitution at the seventh carbon position. Its chemical properties allow it to participate in various reaction types, such as SN2 or SN1 mechanisms, depending on the reaction conditions. This versatility makes it a valuable tool for chemists seeking to explore different synthetic pathways.

In Indonesian laboratories, Ethyl 7-Bromoheptanoate is frequently used in organic chemistry research, particularly in the synthesis of aromatic compounds and long-chain molecules. It is also utilized in educational settings to teach reaction mechanisms and the reactivity of organic compounds. Its application supports both research and teaching, making it an essential component in chemical laboratories across Indonesia.

  • Synthesis of aromatic compounds through bromo substitution reactions, as the compound provides a stable bromo group for further functionalization.
  • Organic synthesis involving long carbon chains, where Ethyl 7-Bromoheptanoate acts as a precursor for chain extension and structural modification.
  • Educational experiments demonstrating SN2 and SN1 reaction mechanisms, due to its predictable reactivity and structural simplicity.
  • Development of new chemical intermediates in research projects requiring brominated functional groups for further synthetic transformations.
  • Preparation of substituted esters for use in pharmaceutical or industrial applications, leveraging its reactivity and structural versatility.

Brand TCI
CAS number 29823-18-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Liquid
Storage Store in a cool, dry place away from light

Ethyl 7-Bromoheptanoate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and moisture. Due to its chemical reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with incompatible materials such as strong bases or oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling ensure the stability and safety of the material in laboratory settings.

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