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TCI

CAS 2491-74-9

4'-Nitro-4-dimethylaminoazobenzene TCI N0192

4'-Nitro-4-dimethylaminoazobenzene TCI N0192

Chemical Identity

CAS No.
2491-74-9
PubChem
CID 17225·SID 87573566
Formula
C14H14N4O2
Molecular weight
270.29 g/mol
Purity
>98.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N,N-dimethyl-4-[(4-nitrophenyl)diazenyl]aniline
SMILES
CN(C)C1=CC=C(C=C1)N=NC2=CC=C(C=C2)[N+](=O)[O-]
InChIKey
LSFRFLVWCKLQTO-UHFFFAOYSA-N
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4'-Nitro-4-dimethylaminoazobenzene is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. It serves as a key building block in organic chemistry, particularly in reactions involving azo bonds (-N=N-). This compound is essential for researchers aiming to create heterocyclic compounds and other organic derivatives due to its unique molecular structure. Its presence in azo reactions allows for the formation of stable intermediates, making it a versatile reagent in synthetic pathways.

The compound's reactivity and polar characteristics stem from its molecular structure, which includes a nitro group and a dimethylamino group. These functional groups contribute to its ability to participate in various chemical reactions, such as substitution, redox, and condensation reactions. Its predictable chemical behavior and stability under controlled conditions make it a preferred choice for synthetic chemists. The compound's polarity and reactivity also enable it to be used in a range of experimental setups, enhancing its utility in both academic and industrial research.

In Indonesian laboratories, 4'-Nitro-4-dimethylaminoazobenzene is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and pharmaceutical applications. Its role in studying azo reactivity and its impact on chemical behavior makes it a valuable material for researchers exploring new synthetic routes and molecular structures. The compound's versatility and reliability in controlled environments ensure its continued use in both educational and research settings.

  • Organic synthesis of heterocyclic compounds due to its reactivity and ability to form azo bonds.
  • Azo reaction studies to investigate the formation and stability of azo intermediates.
  • Pharmaceutical research for the development of new drug molecules with specific functional groups.
  • Redox reaction experiments to explore the compound’s electron transfer properties.
  • Structural analysis in chemical research to understand molecular behavior and reactivity patterns.

Brand TCI
CAS number 2491-74-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid (exact form may vary depending on supplier)
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper disposal in accordance with local regulations. General laboratory safety practices should always be followed when working with this material to ensure a safe and controlled environment.

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