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2-(Dimethylamino)benzaldehyde

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Identification
Molecular formula
C9H11NO
CAS number
99-97-8
IUPAC name
2-(dimethylamino)benzaldehyde
State
State
Solid at room temperature. It is typically handled as a pure substance in its solid form, being stable under standard laboratory conditions.
Melting point (Celsius)
73.00
Melting point (Kelvin)
346.15
Boiling point (Celsius)
302.00
Boiling point (Kelvin)
575.15
General information
Molecular weight
149.19g/mol
Molar mass
149.1900g/mol
Density
1.0790g/cm3
Appearence

2-(Dimethylamino)benzaldehyde appears as a yellow to orange crystalline solid. It may present a faint aromatic odor characteristic of organic aromatic compounds. Its crystalline nature can be observed under a microscope, showing well-formed structures.

Comment on solubility

Solubility of 2-(dimethylamino)benzaldehyde

2-(dimethylamino)benzaldehyde, often referred to by its IUPAC name, is an intriguing organic compound known for its unique solubility properties. Solubility can vary greatly based on several factors, such as temperature and the nature of solvents.

In general, the solubility of 2-(dimethylamino)benzaldehyde can be described as follows:

  • Polar Solvents: This compound exhibits good solubility in polar solvents like water and methanol. The presence of the dimethylamino group allows for favorable interactions with polar molecules.
  • Non-Polar Solvents: It shows limited solubility in non-polar solvents due to the lack of sufficient interactions. Solvents like hexane or cyclohexane are typically not effective for dissolving this compound.
  • Temperature Dependence: As with many organic compounds, solubility may increase with rising temperature, allowing for higher concentrations in solution.

In summary, 2-(dimethylamino)benzaldehyde is more soluble in polar environments, and understanding its solubility behavior is key for applications in synthesis and chemical reactions. Remember: the choice of solvent can significantly influence the reactivity and behavior of this compound.

Interesting facts

Interesting Facts about 2-(Dimethylamino)benzaldehyde

2-(Dimethylamino)benzaldehyde is a fascinating compound that offers a variety of intriguing aspects both in its chemistry and applications. This organic compound is known for its role as a building block in the synthesis of various pharmaceuticals and agrochemicals. Here are some notable characteristics:

  • Structure and Composition: The compound features a benzaldehyde functional group, which gives it unique reactivity and properties. The dimethylamino group acts as a strong electron donor, affecting the overall reactivity.
  • Synthetic Applications: It is widely used in the production of dyes and pigments. Additionally, it serves as an intermediate in the synthesis of other organic compounds, particularly in medicinal chemistry.
  • Reactivity: The presence of both the aldehyde and dimethylamino groups makes this compound reactive in various chemical reactions. It can undergo electrophilic substitution reactions, readily reacting with nucleophiles.
  • Biological Activities: Research has indicated that derivatives of 2-(dimethylamino)benzaldehyde may exhibit interesting biological activities, including potential anti-cancer properties, making it a topic of interest in pharmacological studies.

In essence, 2-(Dimethylamino)benzaldehyde is not just another compound; it is a pivotal component in ongoing chemical research and industrial applications. As scientists continue to explore its potential, it remains a subject of great importance in both organic synthesis and medicinal chemistry.

Synonyms
2-(dimethylamino)benzaldehyde
579-72-6
28602-27-9
Benzaldehyde, (dimethylamino)-
DTXSID60871859
RefChem:561314
DTXCID20819474
673-055-7
2-(N,N-Dimethylamino)benzaldehyde
MFCD03407377
(DIMETHYLAMINO)BENZALDEHYDE
2-dimethylaminobenzaldehyde
2-N,N-(Dimethylamino)benzaldehyde
dimethylaminobenzaldehyd
dimethylamino benzaldehyde
2-dimethylamino-benzaldehyde
N,N-Dimethylaminobenzaldehyde
o-(dimethylamino)benzaldehyde
SCHEMBL97296
SCHEMBL97297
2-(dimethylamino) benzaldehyde
SCHEMBL29954357
DGPBVJWCIDNDPN-UHFFFAOYSA-
AAA57972
SBB086645
AKOS000260541
PS-3643
SY122831
DB-354954
CS-0062404
EN300-66982
F017275
Z335439980
InChI=1/C9H11NO/c1-10(2)9-6-4-3-5-8(9)7-11/h3-7H,1-2H3