Skip to main content

3,5-Dimethoxybenzonitrile

ADVERTISEMENT
Identification
Molecular formula
C9H9NO2
CAS number
673-08-5
IUPAC name
3,5-dimethoxybenzonitrile
State
State
At room temperature, 3,5-Dimethoxybenzonitrile is in a solid state, typically seen as a crystalline powder.
Melting point (Celsius)
78.00
Melting point (Kelvin)
351.15
Boiling point (Celsius)
294.00
Boiling point (Kelvin)
567.15
General information
Molecular weight
161.17g/mol
Molar mass
161.1690g/mol
Density
1.1420g/cm3
Appearence

3,5-Dimethoxybenzonitrile appears as a white to off-white crystalline powder. It is noteworthy for its fine crystalline structure and is often described as having a slightly aromatic odor, typical of benzene derivatives with methoxy functional groups.

Comment on solubility

Solubility of 3,5-Dimethoxybenzonitrile

3,5-Dimethoxybenzonitrile, with the chemical formula C10H11NO2, presents interesting solubility characteristics worth noting:

  • Solvent Preferences: This compound is primarily soluble in organic solvents such as methanol, ethanol, and acetone.
  • Water Solubility: It exhibits low solubility in water, which can be attributed to the hydrophobic nature of the aromatic ring.
  • Temperature Dependence: The solubility in organic solvents often increases with temperature, making warm solvents preferable for effective dissolution.

Overall, the solubility of 3,5-dimethoxybenzonitrile clearly demonstrates the influence of molecular structure on solubility behavior. As often quoted in chemistry, “Like dissolves like,” indicating that compounds similar in polarity tend to dissolve more readily in one another. Hence, knowing the solubility characteristics is crucial for applications in synthesis, formulations, and other chemical processes.

Interesting facts

Interesting Facts about 3,5-Dimethoxybenzonitrile

3,5-Dimethoxybenzonitrile is a fascinating compound that carries unique properties and applications in the field of organic chemistry. It is particularly known for its role in the synthesis of various pharmaceuticals and agrochemicals.

Key Characteristics

  • Functional Groups: This compound features two methoxy (-OCH3) groups and a nitrile group (-CN), which contribute to its reactivity and versatility in chemical reactions.
  • Building Block: Due to its stable aromatic framework, it is often utilized as a building block in the synthesis of more complex organic molecules.
  • Biological Activity: There are ongoing studies focusing on its potential biological activities, paving the way for new pharmaceuticals.

Applications

  • Synthetic Intermediates: It serves as an intermediate in the production of dyes and pigments.
  • Medicinal Chemistry: Research is investigating its role in the creation of drugs that may target various diseases.

As a chemist, it's crucial to appreciate the significance of compounds like 3,5-dimethoxybenzonitrile. Its structural properties make it a prime candidate for various synthetic applications, described by some as "the backbone of innovative chemistry." Understanding compounds such as this one can lead to breakthroughs in science and technology that could benefit various industries.


Synonyms
3,5-Dimethoxybenzonitrile
19179-31-8
BENZONITRILE, 3,5-DIMETHOXY-
EINECS 242-858-0
8OJ1LY7B4L
NSC 73710
BRN 0776115
NSC-73710
1-(Cyanomethyl)-3,5-dimethoxybenzene
DTXSID40172710
3-10-00-01449 (Beilstein Handbook Reference)
DTXCID0095201
242-858-0
RefChem:427518
MFCD00001804
3,5-dimethoxybenzenecarbonitrile
3,5-Dimethoxy benzonitrile
NSC73710
Benzonitrile,5-dimethoxy-
UNII-8OJ1LY7B4L
3,5-dimethoxybenzo nitrile
SCHEMBL202404
SCHEMBL1715885
3,5-Dimethoxybenzonitrile, 99%
BCP11277
SBB008557
AKOS008969358
CS-W001927
FD31244
FS-3228
AC-16561
SY030126
DB-001249
NS00026253
ST50308257
EN300-176374
Z57899965
F0001-0691
InChI=1/C9H9NO2/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-5H,1-2H