4-tert-Butylcyclohexanone TCI B1074

Chemical Identity

CAS No.: 98-53-3
PubChem: CID 7392·SID 87564018
Formula: C10H18O
Molecular weight: 154.25 g/mol
Purity: >97.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-tert-butylcyclohexan-1-one
SMILES: CC(C)(C)C1CCC(=O)CC1
InChIKey: YKFKEYKJGVSEIX-UHFFFAOYSA-N

Rp 1.618.050,00

~~Rp 1.146.600,00~~ Rp 1.618.050,00

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4-Tert-Butylcyclohexanone is an organic compound widely utilized in chemical reactions for the synthesis of complex molecules. As a building block in the field of chemistry, it serves as a fundamental component in the development of various chemical structures. Its cyclic structure and carbonyl group make it a versatile intermediate in synthetic pathways. This compound is commonly found in chemical laboratories as a starting material or a structural building block, offering a stable yet reactive platform for further chemical modifications.

The chemical stability and moderate reactivity of 4-Tert-Butylcyclohexanone make it a preferred choice for a range of laboratory applications. It is suitable for reactions such as reduction, oxidation, and substitution, which are essential in organic synthesis. The presence of the tert-butyl group enhances its utility in protecting functionalities and directing reaction pathways. Its cyclic nature also facilitates the incorporation of various functional groups, making it a valuable tool in the synthesis of heterocyclic compounds and substituted derivatives.

In Indonesian laboratories, 4-Tert-Butylcyclohexanone is extensively used in organic chemistry research, particularly in the synthesis of new compounds and the modification of existing organic structures. It is also commonly employed in educational settings to train students in the practical aspects of chemical synthesis and reaction mechanisms. Its reliability and adaptability make it a staple in both academic and industrial chemical research environments.

Related TCI products

Organic synthesis of complex molecules due to its cyclic structure and carbonyl functionality.
Preparation of substituted derivatives through selective chemical modifications.
Use in reduction and oxidation reactions for functional group transformations.
Application in the synthesis of heterocyclic compounds as a structural building block.
Educational use in teaching chemical reaction mechanisms and synthetic strategies.

Brand	TCI
CAS number	98-53-3
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

4-Tert-Butylcyclohexanone should be stored in a cool, dry location away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and evaporation. Due to its reactive nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to heat or open flames, as the compound may react with certain substances. Proper storage and handling ensure the safety of laboratory personnel and the integrity of the compound during experimentation.

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