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TCI

CAS 1694-31-1

tert-Butyl Acetoacetate TCI A0816

tert-Butyl Acetoacetate TCI A0816

Chemical Identity

CAS No.
1694-31-1
PubChem
CID 15538·SID 87562341
Formula
C8H14O3
Molecular weight
158.19 g/mol
Purity
>95.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl 3-oxobutanoate
SMILES
CC(=O)CC(=O)OC(C)(C)C
InChIKey
JKUYRAMKJLMYLO-UHFFFAOYSA-N
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Tert-Butyl Acetoacetate is a chemical compound widely used as a building block in various laboratory reactions. It serves as a versatile reagent in organic chemistry, particularly in the synthesis of esters, ketones, and other complex molecules. Its stability and reactivity make it a valuable tool for chemists seeking to modify molecular structures efficiently. This compound is commonly found in both academic and industrial research settings, where it plays a key role in the development of new chemical compounds and materials.

The chemical properties of Tert-Butyl Acetoacetate make it a preferred choice for laboratory applications. It exhibits good solubility in organic solvents, which facilitates its use in a wide range of reaction conditions. Additionally, its ability to participate in substitution and elimination reactions enhances its utility in synthetic pathways. The compound’s relatively high boiling point also allows for controlled heating and cooling processes during experiments, ensuring precision in chemical synthesis. These characteristics contribute to its popularity among researchers working in organic chemistry and heterocyclic synthesis.

In Indonesian laboratories, Tert-Butyl Acetoacetate is frequently used in organic chemistry research, especially in educational and research programs focused on the synthesis of new compounds. It is an essential component of the basic laboratory supply, supporting both teaching and experimental activities. Its reliability and ease of handling make it a staple in laboratories that are continuously developing their chemical research capabilities.

  • Organic synthesis experiments benefit from Tert-Butyl Acetoacetate due to its reactivity and solubility in organic solvents, enabling efficient compound formation.
  • Heterocyclic compound development utilizes this reagent for its ability to participate in substitution and elimination reactions, aiding in complex molecule construction.
  • Educational laboratory settings rely on this compound for teaching fundamental chemical reactions and synthesis techniques to students.
  • Industrial research applications use Tert-Butyl Acetoacetate for its stability and versatility in creating new materials and chemical intermediates.
  • Molecular modification processes leverage the compound’s chemical properties to alter molecular structures with precision and control.

Brand TCI
CAS number 1694-31-1
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

Tert-Butyl Acetoacetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent evaporation and contamination. Due to its flammable nature, it should be stored away from heat sources and open flames. Proper ventilation is essential when handling this substance to minimize exposure to vapors. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Regular inspection of storage conditions ensures the compound remains safe and effective for use in chemical experiments.

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