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2-(3-Methylanilino)acetonitrile

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Identification
Molecular formula
C9H10N2
CAS number
22064-85-1
IUPAC name
2-(3-methylanilino)acetonitrile
State
State

At room temperature, 2-(3-Methylanilino)acetonitrile is in a solid state, existing as a crystalline solid which may be white or slightly off-white in color.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.10
Boiling point (Celsius)
385.40
Boiling point (Kelvin)
658.60
General information
Molecular weight
144.19g/mol
Molar mass
144.1870g/mol
Density
1.0600g/cm3
Appearence

2-(3-Methylanilino)acetonitrile appears as a white to off-white crystalline solid. It is typically found in powdered form and is used in various organic synthesis applications.

Comment on solubility

Solubility Profile of 2-(3-methylanilino)acetonitrile

The solubility of 2-(3-methylanilino)acetonitrile can be understood through several important factors:

  • Polarity: The presence of both polar and non-polar functional groups in the molecule significantly influences its solubility in various solvents.
  • Solvent Choice: This compound is likely to be more soluble in polar solvents such as water and ethanol than in non-polar solvents due to its polar acetonitrile group.
  • Hydrogen Bonding: The ability of 2-(3-methylanilino)acetonitrile to engage in hydrogen bonding with solvent molecules enhances its solubility in polar environments.

Given these factors, it can be reasoned that while the compound exhibits moderate solubility in water, its solubility may vary with temperature and concentration.

As a general observation, "like dissolves like," so explore solvent systems that match the compound's functional groups for optimal solubility outcomes.

Interesting facts

Interesting Facts about 2-(3-Methylanilino)acetonitrile

2-(3-Methylanilino)acetonitrile, a compound with unique characteristics, holds significant importance in various fields of study. Here are some intriguing insights:

  • Synthetic Applications: This compound is frequently utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, showcasing its versatility in organic synthesis.
  • Biological Relevance: Compounds like 2-(3-methylanilino)acetonitrile often exhibit biological activity, making them valuable in drug discovery and development.
  • Functional Group Diversity: The presence of both an acetonitrile group and an aniline derivative adds to the compound's reactivity and the range of potential reactions it can undergo, opening doors for further chemical innovations.
  • Research Interest: Chemists and researchers are increasingly interested in studying the compound due to its potential applications in developing new materials and drugs.

As emphasized in many chemistry texts, *“The study of organic compounds is not just about understanding their structure, but also about exploring their potential transformations and applications.”* Therefore, the investigation into compounds like 2-(3-methylanilino)acetonitrile is a crucial pursuit in advancing both academic and practical chemistry.


In conclusion, 2-(3-methylanilino)acetonitrile is more than just a compound; it represents a blend of chemistry, biology, and innovation that continues to inspire researchers around the world.

Synonyms
ACETONITRILE, m-TOLUIDINO-
m-Tolylaminoacetonitrile
28354-22-5
Acetonitrile, m-tolylamino-
BRN 2638752
DTXSID60182598
RefChem:316857
DTXCID00105089
2-(3-methylanilino)acetonitrile
m-Toluidinoacetonitrile
SCHEMBL11269588
AKOS000253442