Interesting facts
Interesting Facts About Methyl N-(3,4-dichlorophenyl)carbamate
Methyl N-(3,4-dichlorophenyl)carbamate is a fascinating compound that draws attention in both the fields of chemistry and agriculture. Here are some key points that highlight its significance:
- Uses in Agriculture: This compound is primarily known for its role as a pesticide. It acts effectively against various pests that threaten crops, making it a valuable tool for farmers.
- Mechanism of Action: Methyl N-(3,4-dichlorophenyl)carbamate works by inhibiting the enzyme acetylcholinesterase, disrupting the normal function of neurotransmitters in pests. This action contributes to its efficacy as a pesticide.
- Environmental Considerations: As with many chemical pesticides, the environmental impact of methyl N-(3,4-dichlorophenyl)carbamate is a topic of ongoing research. Balancing effectiveness with ecological safety is crucial for sustainable agricultural practices.
- Structural Significance: The presence of chlorine atoms in the compound's structure enhances its lipophilicity, which affects its biological activity and stability. This also makes it of interest in medicinal chemistry.
- Research and Development: Continued studies on methyl N-(3,4-dichlorophenyl)carbamate seek to understand its long-term effects and explore potential alternatives that might minimize environmental risks.
In essence, methyl N-(3,4-dichlorophenyl)carbamate exemplifies the complex relationship between chemistry, agriculture, and environmental science. Scientists and researchers are continuously striving to optimize its use while minimizing potential adverse effects on ecosystems.
Synonyms
Methyl N-(3,4-dichlorophenyl)carbamate
Methyl 3,4-dichlorocarbanilate
Carbamic acid, N-(3,4-dichlorophenyl)-, methyl ester
Swep compound
6A0988TW71
WOZQBERUBLYCEG-UHFFFAOYSA-
NIA 2995
inchi=1/c8h7cl2no2/c1-13-8(12)11-5-2-3-6(9)7(10)4-5/h2-4h,1h3,(h,11,12)
SWEP
1918-18-9
NIA 2995J
Methyl 3,4-dichlorophenylcarbamate
Carbamic acid, (3,4-dichlorophenyl)-, methyl ester
FMC 2995
NIA 2,995
3,4-Dichlorocarbanilic acid methyl ester
Carbanilic acid, 3,4-dichloro-, methyl ester
methyl (3,4-dichlorophenyl)carbamate
Methylester kyseliny 3,4-dichlorkarbanilove
DTXSID7042437
CHEBI:82188
Caswell No. 818
Swep [ANSI]
HSDB 1770
EPA Pesticide Chemical Code 084601
BRN 2805600
Methyl-N-(3,4-dichlorophenyl) carbamate
UNII-6A0988TW71
Methylester kyseliny 3,4-dichlorkarbanilove [Czech]
N-(3,4-dichlorophenyl)-carbamic acid-methyl ester
SWEP [HSDB]
SCHEMBL116096
CHEMBL1573885
DTXCID5022437
Swep (N-(3,4-dichlorophenyl)carbamic acid-methyl ester)
BDBM85224
methyl 3,4-dichlorophenyl carbamate
Tox21_301335
STK695731
AKOS003442078
NCGC00166197-01
NCGC00255980-01
Swep, PESTANAL(R), analytical standard
CAS-1918-18-9
CAS_1918-18-9
DB-044777
3,4-Dichlorophenylcarbamic acid methyl ester
CS-0361653
NS00004382
C19062
Q27155793
Solubility of Methyl N-(3,4-dichlorophenyl)carbamate
Methyl N-(3,4-dichlorophenyl)carbamate, commonly known by its systematic name, possesses unique solubility characteristics that merit close examination. This compound is classified as a carbamate, which influences its solubility profile due to the presence of both hydrophilic and hydrophobic elements within its structure.
Generally, the solubility of carbamates can vary greatly depending on the substituents attached to the core structure. In the case of methyl N-(3,4-dichlorophenyl)carbamate, consider the following:
Overall, the solubility of methyl N-(3,4-dichlorophenyl)carbamate can be summarized as:
As with many synthetic compounds, the solubility behavior can be influenced by environmental factors such as temperature and pH, reinforcing the need for careful consideration when predicting its behavior in various contexts. In conclusion, understanding the solubility of methyl N-(3,4-dichlorophenyl)carbamate is crucial for its application in fields such as pharmaceuticals and agrochemicals.