Interesting facts
Exploring 1-(Chloromethyl)-3-methyl-benzene
1-(Chloromethyl)-3-methyl-benzene, often referred to as a derivative of toluene, exhibits unique characteristics that are of significant interest in both industrial and academic settings. Here are some fascinating aspects about this compound:
- Structure and Isomerism: This compound features a chloromethyl group (-CH2Cl) attached to a toluene fragment, highlighting its role as a versatile intermediate in organic synthesis. The presence of the methyl group in the meta position introduces interesting isomeric forms that can influence its reactivity and properties.
- Synthesis and Applications: 1-(Chloromethyl)-3-methyl-benzene can be synthesized through various methods, including electrophilic aromatic substitution. Its application as a building block in the production of pharmaceuticals, agrochemicals, and specialized polymers makes it valuable in industrial chemistry.
- Reactivity and Functionalization: Due to the chloromethyl group, this compound can undergo reactions such as nucleophilic substitution and can participate in Friedel-Crafts reactions. This reactivity allows chemists to introduce different functional groups, expanding its utility in organic synthesis.
- Environmental Considerations: As with many chlorinated compounds, there are concerns regarding the environmental impact and potential toxicity of 1-(Chloromethyl)-3-methyl-benzene. Understanding the behavior of this compound in the environment is crucial for developing safer handling practices and regulations.
- In Research: Chemical research involving 1-(Chloromethyl)-3-methyl-benzene is focused on enhancing its synthesis methods and finding more efficient pathways for functionalization. Research on similar chlorinated benzenes can yield insights into the development of new materials.
As a valuable compound both in the laboratory and in industrial applications, 1-(Chloromethyl)-3-methyl-benzene continues to capture the attention of scientists aiming to unlock its full potential. Its properties and versatile reactivity make it a worthwhile subject of study for anyone interested in organometallic and synthetic chemistry.
Synonyms
3-Methylbenzyl chloride
620-19-9
1-(chloromethyl)-3-methylbenzene
m-Xylyl chloride
m-Methylbenzyl chloride
Benzene, 1-(chloromethyl)-3-methyl-
m-(Chloromethyl)toluene
3-(Chloromethyl)toluene
ALPHA-CHLORO-M-XYLENE
.alpha.-Chloro-m-xylene
m-Xylyl-.alpha.-chloride
m-Xylyl-alpha-chloride
3-methylphenylmethyl chloride
NSC 76592
1-Methyl-3-chloromethylbenzene
m-Xylene, alpha-chloro-
EINECS 210-628-9
NSC-76592
771291VTT8
M-XYLYL CHLORIDE [MI]
.OMEGA.-CHLORO-M-XYLENE
DTXSID60211034
OMEGA-CHLORO-M-XYLENE
m-Xylene, alpha-chloro-(8CI)
DTXCID60133525
Benzene, 1-(chloromethyl)-3-methyl-(9CI)
210-628-9
3-Methylbenzylchloride
m-Xylene, .alpha.-chloro-
1-(chloromethyl)-3-methyl-benzene
3-methyl benzyl chloride
A-CHLORO-M-XYLENE
m-Xylylchlorid
UNII-771291VTT8
MFCD00000909
3-metylbenzyl chloride
.alpha.-Chloro-meta-xylene
SCHEMBL52147
1-Chloromethyl-3-methylbenzene
ghl.PD_Mitscher_leg0.1073
3-Methylbenzyl chloride, 98%
1-chloromethyl-3-methyl-benzene
LZBOHNCMCCSTJX-UHFFFAOYSA-
NSC76592
STR01886
STL141071
AKOS000121524
DB-054041
NS00034893
EN300-21165
E76481
Q27266528
F2190-0260
InChI=1/C8H9Cl/c1-7-3-2-4-8(5-7)6-9/h2-5H,6H2,1H3
Solubility of 1-(Chloromethyl)-3-methyl-benzene
1-(Chloromethyl)-3-methyl-benzene, also known as p-Chlorotoluene, exhibits intriguing solubility characteristics due to its chemical structure. The compound's solubility can be influenced by various factors, including:
In summary, while 1-(Chloromethyl)-3-methyl-benzene is soluble in organic solvents, it shows negligible solubility in water. This characteristic is significant for applications that rely on solvent selection, making it essential to choose appropriate solvents for dissolution and reactions. As the saying goes, “like dissolves like,” and understanding the solubility of this compound is crucial for effective chemical processes.