Interesting facts
Exciting Facts About (2-sec-butylphenyl) N-methylcarbamate
(2-sec-butylphenyl) N-methylcarbamate is a fascinating compound that falls within the class of carbamates, known for their wide range of applications in agriculture, pharmaceuticals, and beyond. Here are some notable aspects that make this compound intriguing:
- Structural Diversity: This compound exhibits structural diversity due to the presence of the sec-butyl group attached to a phenyl ring. This configuration can influence its reactivity and overall properties, making it a valuable compound in organic synthesis and design.
- Biological Significance: Carbamates, including this compound, often serve as effective inhibitors of enzymes like acetylcholinesterase. This means they can play significant roles in the development of pesticides and pharmaceuticals that target neurological systems.
- Potential Applications: The unique structure of (2-sec-butylphenyl) N-methylcarbamate lends itself to potential applications as an agrochemical. These compounds are frequently used to enhance crop protection by controlling pests without harming beneficial insects.
- Research Interest: There is ongoing research into the pharmacological aspects of carbamates, with studies exploring their potential as anti-inflammatory and neuroprotective agents. The modifications in their structure can lead to new therapeutic pathways.
- Environmental Considerations: As with many chemical compounds, understanding its environmental impact is crucial. Research into the degradation and toxicity of carbamates helps to ensure they can be used safely in various applications, especially in agriculture.
In conclusion, (2-sec-butylphenyl) N-methylcarbamate exemplifies how small changes in molecular structure can lead to diverse properties and applications. As scientists explore its potential, this compound remains a testament to the significance of carbamate chemistry in both industrial and academic realms.
Synonyms
Fenobucarb
3766-81-2
Baycarb
Bassa
2-sec-Butylphenyl N-methylcarbamate
Barizon
Fenobcarb
Carvil
Hopcin
Osbac
2-sec-Butylphenyl methylcarbamate
2-(1-Methylpropyl)phenyl methylcarbamate
Bayer 41367C
Geocarb 50EC
Bayer 41637
Phenol, 2-(1-methylpropyl)-, methylcarbamate
Fenobucarb [BSI:ISO]
BAY 41637
Methylcarbamic acid o-sec-butylphenyl ester
o-sec-Butylphenyl methylcarbamate
Carbamic acid, methyl-, o-sec-butylphenyl ester
EINECS 223-188-8
5MS2P7M0CF
2-(butan-2-yl)phenyl methylcarbamate
2-Butylphenyl methylcarbamate
BRN 2052332
CHEBI:34304
AI3-27212
FENOBUCARB [ISO]
2-sek.Butylfenylester kyseliny methylkarbaminove
Phenol, 2-(1-methylpropyl)-, 1-(N-methylcarbamate)
2-sek.Butylfenylester kyseliny methylkarbaminove [Czech]
DTXSID4058077
BAY-41637
2-(butan-2-yl)phenyl N-methylcarbamate
(+-)-FENOBUCARB
FENOBUCARB, (+-)-
DTXCID0031845
223-188-8
BPMC
(2-butan-2-ylphenyl) N-methylcarbamate
MFCD00053081
2-sec-Butylphenyl-N-methylcarbamate
Fenobucarb 10 microg/mL in Cyclohexane
2-(Sec-butyl)phenyl methylcarbamate
UNII-5MS2P7M0CF
baycarb (tm)
o-sec-butylphenyl n-methylcarbamate
Fenobucarb (Standard)
(+/-)-FENOBUCARB
SCHEMBL73674
CHEMBL226650
DIRFUJHNVNOBMY-UHFFFAOYSA-
FENOBUCARB, (+/-)-
HY-B0835R
2-sec butylphenyl N-methylcarbamate
HY-B0835
2-Sec-butylphenyl methylcarbamate #
2-Sec. butylphenyl N-methylcarbamate
AKOS015960925
AS-76198
SY110156
DB-049163
CS-0012849
NS00009809
Fenobucarb, PESTANAL(R), analytical standard
Methyl-carbamic acid 2-sec-butyl-phenyl ester
Q3268119
InChI=1/C12H17NO2/c1-4-9(2)10-7-5-6-8-11(10)15-12(14)13-3/h5-9H,4H2,1-3H3,(H,13,14)
Solubility of (2-sec-butylphenyl) N-methylcarbamate
(2-sec-butylphenyl) N-methylcarbamate is a chemical compound that exhibits interesting solubility characteristics, which are important for both its practical applications and theoretical considerations. The solubility of organic compounds like this one can be influenced by several factors:
Furthermore, it has been noted that "like dissolves like," which indicates that the solvent's chemical nature can affect solubility outcomes. Therefore, while this compound can be expected to demonstrate some solubility in aqueous solutions due to its functional groups, it will likely achieve greater solubility in organic solvents due to its hydrophobic characteristics. Understanding these solubility properties is crucial for applications in pharmaceuticals and agrochemicals.