Interesting facts
Interesting Facts about 2-Chloro-6-methyl-aniline
2-Chloro-6-methyl-aniline, often referred to in the chemical community as a key derivative of aniline, is prized for its versatility in organic synthesis and industrial applications. Here are some noteworthy aspects of this intriguing compound:
- Structural Significance: This compound features a chloro group (Cl) and a methyl group (CH₃) on the aniline structure, which influences its reactivity and properties. The position of these substituents can significantly impact the compound's chemical behavior, making it a subject of study in various fields.
- Use in Dyes: One of the primary applications of 2-chloro-6-methyl-aniline is in the manufacture of azo dyes. Azo compounds are renowned for their vibrant colors and are extensively used in textiles, inks, and plastics.
- Synthesis Pathways: The synthesis of 2-chloro-6-methyl-aniline can be accomplished through various methods, including the chlorination of 6-methyl-aniline. Chemists often explore multiple routes to optimize yield and reduce environmental impact during industrial production.
- Biological Relevance: As with many aniline derivatives, 2-chloro-6-methyl-aniline has garnered attention in the field of medicinal chemistry. Research has indicated its potential interactions with biological systems, including studies focusing on its effects on enzymes and cellular activities.
- Safety Considerations: Like many aromatic amines, handling this compound requires caution; it may pose health risks such as skin and eye irritation, and it is vital to follow appropriate safety protocols when working with it in a laboratory setting.
As an essential building block in various chemical processes, 2-chloro-6-methyl-aniline continues to capture the interest of chemists due to its functional versatility and application potential. In the words of a renowned chemist, "The linchpins of chemistry lie in the bonds we create; each compound tells a story of possibilities."
Synonyms
2-Chloro-6-methylaniline
87-63-8
6-Chloro-o-toluidine
2-Amino-3-chlorotoluene
6-CHLORO-2-METHYLANILINE
Benzenamine, 2-chloro-6-methyl-
3-Chloro-2-aminotoluene
2-Methyl-6-chloroaniline
6-Chloro-2-toluidine
o-Toluidine, 6-chloro-
2-CHLORO-6-METHYL-ANILINE
6-Chloro-o-toluidine (NH2=1)
EINECS 201-759-2
UNII-76F11RQ7TB
NSC 60121
BRN 0774624
Benzenamine, 6-chloro-2-methyl-
NSC-60121
2-chloro-6-methylbenzenamine
76F11RQ7TB
(2-Chloro-6-methylphenyl)amine
DTXSID8058956
4-12-00-01789 (Beilstein Handbook Reference)
6-Chloro-o-toluidine [NH2=1]
6-chloro-2-methyl aniline
2-chloro-6-methylphenylamine
NSC60121
MFCD00007679
6-Chlor-ortho-toluidin
2-chloro-6-methyl aniline
WLN: ZR BG F1
SCHEMBL94065
6-chloro-2-methylbenzenamine
2-chloranyl-6-methyl-aniline
2-chloro-6-methyl-phenylamine
DTXCID0048553
2-Chloro-6-methylaniline, 98%
CS-D1492
GEO-00703
STL164360
AKOS005254415
AC-4800
FC03024
GS-3024
Benzenamine, 6-chloro-2-methyl-(9CI)
BP-13318
A1959
NS00039208
6-Chloro-o-toluidine;2-Amino-3-chlorotoluene
EN300-78799
A842321
Q27266484
(1S)-2-methyl-6-methylidenecyclohexa-2,4-dien-1-amine
2CM
Solubility of 2-chloro-6-methyl-aniline
2-chloro-6-methyl-aniline, also known by its systematic name, can be characterized by its solubility properties, which are primarily influenced by its molecular structure. Solubility in various solvents is crucial for understanding the compound's reactivity and behavior in different environments.
Here are some key points regarding the solubility of 2-chloro-6-methyl-aniline:
In conclusion, the solubility of 2-chloro-6-methyl-aniline depends on a variety of factors, including solvent choice and environmental conditions, which are essential considerations for practical applications in chemical synthesis and industrial processes.