Interesting facts
Interesting Facts about 4-chloro-3-methyl-aniline
4-chloro-3-methyl-aniline is a fascinating aromatic amine that plays a significant role in various fields of chemistry and industry. Here are some engaging details:
- Structure and Reactions: This compound consists of a benzene ring substituted with a chloro group and a methyl group, along with an amino functional group. Its structure allows it to participate in various electrophilic aromatic substitution reactions, highlighting its reactivity in organic synthesis.
- Application in Dyes: One of the most prominent uses of 4-chloro-3-methyl-aniline is in the production of dyes. Its derivatives can produce vibrant colors and are integral in the textile and paint industries. The versatility of this compound allows for the synthesis of different color shades, making it invaluable for manufacturers.
- Biological Interest: Studies have shown that compounds like 4-chloro-3-methyl-aniline can exhibit biological activities. Some research indicates potential antimicrobial properties, which holds promise for further investigations in medicinal chemistry.
- Safety Considerations: As with many aromatic amines, there are important safety considerations when working with this compound. Exposure can pose health risks, including carcinogenic effects, making it crucial to work with appropriate safety measures.
- Environmental Impact: The environmental fate of 4-chloro-3-methyl-aniline is also an area of research interest, especially regarding its persistence and potential toxicity in aquatic environments. Understanding these implications is vital for regulatory compliance in chemical manufacturing.
In conclusion, 4-chloro-3-methyl-aniline is not just a molecule with a rich structure; it is a compound that is entwined with practical applications, biological relevance, and important safety considerations. These attributes make it a noteworthy subject of study in both academic and industrial chemistry.
Synonyms
4-Chloro-3-methylaniline
7149-75-9
5-Amino-2-chlorotoluene
4-Chloro-m-toluidine
Benzenamine, 4-chloro-3-methyl-
m-Toluidine, 4-chloro-
3-METHYL-4-CHLOROANILINE
(4-Chloro-3-methylphenyl)amine
UNII-6Q2W6L7BWZ
6Q2W6L7BWZ
NSC-72329
4-Chloro-3-Methylbenzenamine
2-CHLORO-5-AMINOTOLUENE
DTXSID5073377
HIHCTGNZNHSZPP-UHFFFAOYSA-
NSC 72329
BENZENAMINE, 4-CHLORO-3-METHYL
DTXCID5047039
615-298-3
hihctgnznhszpp-uhfffaoysa-n
inchi=1/c7h8cln/c1-5-4-6(9)2-3-7(5)8/h2-4h,9h2,1h3
MFCD00066332
4-chloro-3-methylphenylamine
4-Chloro-3-methyl-phenylamine
NSC72329
4-Chlor-m-toluidin
4-chloro-3-methyl aniline
4-chloro-3-methyl-aniline
NCIOpen2_000389
4-chloranyl-3-methyl-aniline
SCHEMBL404331
4-Chloro-3-methylaniline, 98%
GEO-00704
STL169112
TD1176
AKOS005259258
CS-W002307
AS-11595
SY011127
DB-024225
NS00037223
EN300-104644
A837210
Q27265310
F0001-1836
Solubility of 4-chloro-3-methyl-aniline
4-chloro-3-methyl-aniline (C7H8ClN) is an organic compound known for its moderate solubility characteristics. Understanding its solubility behavior involves considering various factors:
Overall, the solubility of 4-chloro-3-methyl-aniline can be described as:
In conclusion, the compound's solubility parameters indicate that while it can find utility in various organic reactions, its dissolved state will be notably better suited under non-polar to moderately polar conditions.