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TCI

CAS 104-04-1

4'-Nitroacetanilide TCI N0108

4'-Nitroacetanilide TCI N0108

Chemical Identity

CAS No.
104-04-1
PubChem
CID 7691·SID 87573497
Formula
C8H8N2O3
Molecular weight
180.16 g/mol
Purity
>99.0%(GC)
Reference databases
ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N-(4-nitrophenyl)acetamide
SMILES
CC(=O)NC1=CC=C(C=C1)[N+](=O)[O-]
InChIKey
NQRLPDFELNCFHW-UHFFFAOYSA-N
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4'-Nitroacetanilide is a chemical compound widely used in organic synthesis, particularly in electrophilic substitution reactions. It serves as a key building block in the development of various organic compounds, including heterocyclic structures. Its versatility makes it an essential reagent in chemical laboratories, where it is utilized for its predictable chemical behavior and reactivity. This compound is commonly employed in reactions such as Friedel-Crafts and nitration, contributing to the synthesis of bioactive molecules and industrial chemicals.

The compound’s stable molecular structure and controlled reactivity make it a preferred choice for researchers. It is easily compatible with a range of reagents, allowing for efficient chemical transformations. Its consistent chemical properties ensure reliable results in experimental settings, which is crucial for scientific accuracy. Additionally, its ease of handling and processing in the laboratory further enhance its appeal for both academic and industrial applications.

In Indonesian laboratories, 4'-Nitroacetanilide is frequently used in organic chemistry research, especially in pharmaceutical and material science fields. Its availability in the local market supports ongoing research efforts aimed at developing new compounds with potential medical or industrial applications. Its role in the synthesis of bioactive substances underscores its importance in advancing scientific innovation in the region.

  • Organic synthesis in pharmaceutical research due to its role in creating bioactive compounds.
  • Nitration reactions where it serves as a reactive intermediate for functional group modification.
  • Friedel-Crafts acylation for the formation of aromatic derivatives in compound development.
  • Heterocyclic compound synthesis as a precursor for pharmaceutical and industrial applications.
  • Chemical research in material science for the development of new functional materials.

Brand TCI
CAS number 104-04-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

4'-Nitroacetanilide should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. As a chemical building block, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. It is important to keep it away from incompatible materials such as strong oxidizing agents. Proper labeling and storage conditions help maintain its chemical integrity and ensure safe usage in laboratory settings.

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