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CAS 838-57-3

Ethyl (4-Nitrobenzoyl)acetate TCI N0513

Ethyl (4-Nitrobenzoyl)acetate TCI N0513

Chemical Identity

CAS No.
838-57-3
PubChem
CID 13281·SID 87573838
Formula
C11H11NO5
Molecular weight
237.21 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ethyl 3-(4-nitrophenyl)-3-oxopropanoate
SMILES
CCOC(=O)CC(=O)C1=CC=C(C=C1)[N+](=O)[O-]
InChIKey
NGRXSVFCLHVGKU-UHFFFAOYSA-N
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Ethyl (4-Nitrobenzoyl)acetate is a chemical compound widely used in synthetic reactions within laboratory settings. It belongs to the category of building blocks, which are fundamental components in the synthesis of more complex chemical structures. This compound plays a crucial role in organic chemistry by serving as a substrate or reagent in various reactions such as esterification and substitution. Its stability and controlled reactivity make it a reliable choice for researchers aiming to produce a wide range of chemical derivatives.

The compound’s chemical properties, including its solubility in organic solvents like ethyl acetate and chloroform, facilitate efficient separation and isolation of final products. Its ability to participate in substitution and nucleophilic reactions enhances its utility in the synthesis of heterocyclic and aromatic compounds. These characteristics make it a versatile reagent that supports a variety of experimental approaches in both academic and industrial research environments.

In Indonesian laboratories, Ethyl (4-Nitrobenzoyl)acetate is extensively utilized in organic chemistry research, particularly in higher education institutions and applied research programs. It is commonly employed in the development of new chemical compounds and in teaching practical laboratory techniques. Its availability and reliability make it a preferred choice for both educational and research purposes in the region.

  • Organic synthesis applications benefit from its role as a versatile reagent in esterification and substitution reactions.
  • It is ideal for teaching practical laboratory techniques in higher education institutions due to its predictable chemical behavior.
  • The compound supports the development of heterocyclic and aromatic compounds through nucleophilic substitution reactions.
  • Its solubility in organic solvents makes it suitable for purification and isolation processes in analytical chemistry.
  • It is frequently used in applied research for the synthesis of new chemical derivatives and functional materials.

Brand TCI
CAS number 838-57-3
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 direct sunlight

Ethyl (4-Nitrobenzoyl)acetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and moisture. Due to its organic nature, it is best stored in glass or polyethylene containers that are resistant to chemical degradation. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the workspace to minimize inhalation risks. Regular monitoring of storage conditions helps maintain the integrity of the compound for consistent experimental results.

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