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CAS 5320-91-2

Dimethyl Azobenzene-4,4'-dicarboxylate TCI A1581

Dimethyl Azobenzene-4,4'-dicarboxylate TCI A1581

Chemical Identity

CAS No.
5320-91-2
PubChem
CID 585660·SID 87563023
Formula
C16H14N2O4
Molecular weight
298.29 g/mol
Purity
>95.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 4-[(4-methoxycarbonylphenyl)diazenyl]benzoate
SMILES
COC(=O)C1=CC=C(C=C1)N=NC2=CC=C(C=C2)C(=O)OC
InChIKey
PSNNNVCIKCUWKM-UHFFFAOYSA-N
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Dimethyl Azobenzene-4,4'-dicarboxylate (DMAC) is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it serves as a versatile intermediate that can be modified through various chemical reactions to produce a wide range of derivatives. Its role in the laboratory is critical for researchers working on the development of new compounds, particularly in the fields of pharmaceuticals and materials science. DMAC is valued for its ability to participate in controlled reactions, allowing for precise manipulation of molecular structures.

One of the key properties that make DMAC a preferred choice is its stable chemical structure, which ensures consistent performance across different experimental conditions. Its controlled reactivity allows chemists to tailor reactions to achieve specific outcomes, making it a reliable component in synthetic pathways. Additionally, DMAC is compatible with a variety of reagents and solvents, enhancing its utility in diverse laboratory applications. These characteristics make it an essential tool for researchers aiming to produce high-quality, reproducible results.

In Indonesian laboratories, DMAC is commonly used in organic chemistry research, drug development, and material science projects. Its availability in various packaging options ensures that it can be easily integrated into both small-scale and large-scale experiments. The compound’s stability and predictable behavior make it a trusted choice for scientists seeking reliable and consistent chemical building blocks for their work.

  • Organic synthesis projects benefit from DMAC as it provides a stable and reactive starting point for the creation of complex molecules.
  • Pharmaceutical research utilizes DMAC in the development of new drug compounds due to its compatibility with a wide range of reagents.
  • Material science experiments often incorporate DMAC to create novel materials with specific chemical properties.
  • Chemical education programs use DMAC to teach students about azo compounds and their synthetic applications.
  • Industrial research and development teams rely on DMAC for the production of specialty chemicals and intermediates.

Brand TCI
CAS number 5320-91-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various sizes to suit different laboratory needs
Physical form Solid (exact form may vary depending on supplier)
Storage Store in a cool, dry place away from light and moisture

DMAC should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of materials such as glass or high-density polyethylene to prevent contamination and degradation. In laboratory settings, it is important to handle DMAC with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety during handling. Due to its chemical nature, it should be kept separate from incompatible substances to avoid any potential reactions. Proper labeling and storage practices help ensure the compound remains safe and effective for use in research applications.

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