Interesting facts
Interesting Facts about (3,5-Diisopropylphenyl) N-methylcarbamate
(3,5-Diisopropylphenyl) N-methylcarbamate is a fascinating compound that has garnered attention in the field of organic chemistry. This compound is part of the broader class of carbamates, which are known for their diverse applications in agriculture, industrial processes, and pharmaceuticals. Here are some intriguing points about this compound:
- Mechanism of Action: Carbamates such as this one function typically by inhibiting the enzyme acetylcholinesterase, which plays a pivotal role in the transmission of nerve signals. This mechanism is what makes carbamates effective in pest control, as they disrupt normal neural function in insects.
- Versatility: The unique structure of (3,5-Diisopropylphenyl) N-methylcarbamate provides it with versatile properties, making it suitable for various applications, including insecticides and herbicides.
- Synthetic Interest: Chemists are constantly exploring new synthetic pathways to create derivatives of carbamates, offering potential variations that may enhance efficacy or reduce environmental impact.
- Safety Considerations: Being a member of the carbamate family, this compound is subject to rigorous safety evaluations due to its biological activity. Understanding its toxicity levels and safe handling practices is crucial, especially in agricultural use.
- Regulatory Aspects: As with many chemicals in the agricultural sector, there are stringent regulatory frameworks governing the use of compounds like (3,5-Diisopropylphenyl) N-methylcarbamate. Compliance with these regulations ensures that the compound can be used safely and effectively.
As scientists continue to study (3,5-Diisopropylphenyl) N-methylcarbamate, they pave the way for innovative applications while also addressing the challenges of sustainability and safety. Awareness of its properties and implications contributes to a deeper understanding of chemical compounds and their roles in our world.
Synonyms
Hooker hrs-1422
3,5-Diisopropylphenyl N-methylcarbamate
3,5-Diisopropylphenyl methylcarbamate
330-64-3
DRC 2823
HRS 1422
ENT 25,780
Phenol, 3,5-bis(1-methylethyl)-, methylcarbamate
Phenol, 3,5-diisopropyl-, methylcarbamate
Hooker HRS 1422
VX5THC2XSA
3,5-Bis(1-methylethyl)phenyl methylcarbamate
Carbamic acid, methyl-, 3,5-bis(1-methylethyl)phenyl ester
CARBAMIC ACID, METHYL-, 3,5-DIISOPROPYLPHENYL ESTER
3,5-Bis(1-methylethyl)phenol, methylcarbamate
Caswell No. 356A
EPA Pesticide Chemical Code 356200
BRN 1978356
AI3-25780
HRS-1422
Hooker 1422
UNII-VX5THC2XSA
DTXSID1041471
SCHEMBL11508629
CUTUCYVZTGGYDL-UHFFFAOYSA-N
3,5-diisopropylphenyl n -methylcarbamate
NS00120844
DIISOPROPYLPHENYL METHYLCARBAMATE, 3,5-
Carbamic acid, 3,5-diisopropylphenyl ester, N-methyl
Phenol, 3,5-bis(1-methylethyl)-, 1-(N-methylcarbamate)
Solubility of (3,5-diisopropylphenyl) N-methylcarbamate
(3,5-diisopropylphenyl) N-methylcarbamate is a fascinating compound with unique solubility characteristics. Its solubility is influenced by various factors, including the presence of the isopropyl groups and the carbamate functional group.
To explore its solubility further, consider the following points:
In summary, while (3,5-diisopropylphenyl) N-methylcarbamate may not be highly soluble in all solvents, its unique structure offers intriguing possibilities for solubility in specific organic environments. As noted, "Solubility is not only a physical property but a powerful indicator of molecular interactions." Understanding these solubility traits can pave the way for practical applications in various fields such as pharmaceuticals and agrochemicals.