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Carbosulfan

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Identification
Molecular formula
C20H32N2O3
CAS number
55285-14-8
IUPAC name
[4-(diallylamino)-3,5-dimethyl-phenyl] N-methylcarbamate
State
State

At room temperature, Carbosulfan is typically in a solid state, often sold as a granular formulation for agricultural use.

Melting point (Celsius)
79.00
Melting point (Kelvin)
352.15
Boiling point (Celsius)
418.00
Boiling point (Kelvin)
691.15
General information
Molecular weight
326.49g/mol
Molar mass
326.4200g/mol
Density
1.1700g/cm3
Appearence

Carbosulfan is an off-white to cream-colored solid with a slight aromatic odor. It is typically found in a technical grade form as a solid powder.

Comment on solubility

Solubility of [4-(diallylamino)-3,5-dimethyl-phenyl] N-methylcarbamate

The solubility of the compound [4-(diallylamino)-3,5-dimethyl-phenyl] N-methylcarbamate can vary widely depending on several factors, including temperature, pH, and the presence of solvents. In general, carbamate compounds exhibit diverse solubility profiles that can be characterized as follows:

  • Polar Solvents: This compound is likely to be more soluble in polar solvents such as water and alcohol due to the presence of functional groups that can engage in hydrogen bonding.
  • Non-Polar Solvents: The presence of diallyl groups suggests reduced solubility in non-polar solvents such as hexane or benzene, where steric hindrance may affect interaction.
  • Temperature Effects: Increased temperature typically enhances solubility for many organic compounds, which could be beneficial for applications involving this carbamate.
  • pH Influence: The ionization state of the amino groups can be influenced by pH, potentially altering solubility. For example, at higher pH levels, the amino groups may remain protonated, thereby affecting solubility.

As a rule of thumb, the greater the number of polar functional groups, the higher the solubility in polar environments. It is important to conduct empirical solubility tests for precise insights, especially in the context of pharmacological and industrial applications.

Interesting facts

Exciting Insights on [4-(Diallylamino)-3,5-dimethyl-phenyl] N-methylcarbamate

[4-(Diallylamino)-3,5-dimethyl-phenyl] N-methylcarbamate is a fascinating compound that combines structural complexity with significant biochemical potential. It falls within the category of carbamates, a class known for their applications in various fields, including agriculture and pharmaceuticals.

Key Characteristics

  • Biological Activity: Many carbamate derivatives exhibit *insecticidal and herbicidal properties*, making them essential in crop protection.
  • Research Applications: Compounds like this can be crucial in developing new treatments for neurological disorders, showcasing their versatility in medicinal chemistry.
  • Structural Diversity: The presence of both diallylamino and dimethyl groups contributes to unique reactivity and *stability*, impacting how this compound interacts with biological systems.

Chemical Implications

This compound serves as an *excellent case study* for understanding how subtle changes in molecular structure can lead to significant differences in activity and application. Researchers often study analogs of carbamate structures to explore their efficacy and potential side effects in biological systems.

Future Prospects

As environmental concerns rise, the development of *safer and more effective pesticides* leads to a renewed interest in compounds like [4-(Diallylamino)-3,5-dimethyl-phenyl] N-methylcarbamate. Its synthesis and modification could pave the way for innovations in sustainable agriculture.

In conclusion, this compound embodies the intricate relationship between structure, function, and application in the chemical landscape. The study of such compounds not only enhances our understanding of organic chemistry but also contributes to advancements in environmental and health sciences.

Synonyms
Allyxycarb
6392-46-7
Hydrol
APC (pesticide)
Hydrol (insecticide)
Caswell No. 283A
Allyxycarb [BSI:ISO]
EINECS 229-002-1
BAY 50282
EPA Pesticide Chemical Code 283600
UNII-66S9S03B4N
BRN 2873224
AI3-27109
4-Diallylamino-3,5-xylyl N-methylcarbamate
Phenol, 4-(di-2-propenylamino)-3,5-dimethyl-, methylcarbamate (ester)
4-(Diallylamino)-3,5-xylyl methylcarbamate
66S9S03B4N
A 546
ALLYXYCARB [ISO]
3,5-Dimethyl-4-diallylaminophenyl-N-methylcarbamate
4-Diallylamino-3,5-dimethylphenyl N-methylcarbamate
3,5-Xylenol, 4-(diallylamino)-, methylcarbamate (ester)
DTXSID7041592
CARBAMIC ACID, METHYL-, 4-(DIALLYLAMINO)-3,5-XYLYL ESTER
Phenol, 4-(di-2-propenylamino)-3,5-dimethyl-, methylcarbamate
4-[bis(prop-2-en-1-yl)amino]-3,5-dimethylphenyl N-methylcarbamate
4-DIALLYLAMINO-3,5-XYLYL METHYLCARBAMATE
4-(DI-2-PROPEN-1-YLAMINO)-3,5-DIMETHYLPHENYL N-METHYLCARBAMATE
4-(bis(prop-2-en-1-yl)amino)-3,5-dimethylphenyl N-methylcarbamate
DTXCID5021592
Phenol, 4-(di-2-propenylamino)-3,5-dimethyl-, methylcarbamate (ester) (9CI)
229-002-1
[4-[bis(prop-2-enyl)amino]-3,5-dimethylphenyl] N-methylcarbamate
SCHEMBL117902
CHEBI:82087
FBEHFRAORPEGFH-UHFFFAOYSA-N
AKOS040747794
NS00035604
C18947
Q27155739