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Methomyl

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Identification
Molecular formula
C7H11N3O2
CAS number
16752-77-5
IUPAC name
(5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate
State
State

Methomyl is usually found in a solid state at room temperature. It is often handled as a powder for commercial use, particularly in its role as a pesticide.

Melting point (Celsius)
78.00
Melting point (Kelvin)
351.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
162.18g/mol
Molar mass
162.1800g/mol
Density
0.9700g/cm3
Appearence

Methomyl is typically a white crystalline solid with a slight sulfurous odor. It is commonly formulated as a powder or granules for use in agricultural applications.

Comment on solubility

Solubility of (5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate

The solubility of (5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate can be quite intriguing, as various factors influence its behavior in different solvents.

Key considerations for assessing solubility include:

  • Polarity of the solvent: As a general rule, "like dissolves like." This means that non-polar compounds tend to dissolve better in non-polar solvents.
  • Temperature: Increased temperatures often enhance solubility, as thermal energy can help overcome lattice energy and intermolecular forces.
  • Presence of functional groups: The existence of functional groups in the compound can lead to hydrogen bonding or dipole-dipole interactions, affecting overall solubility.

Because of its specific structure, (5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate may exhibit varying degrees of solubility in organic solvents. Common solvents like ethanol and acetone could facilitate dissolution due to their polar characteristics, while water might present challenges due to the compound's hydrophobic regions.

In conclusion, investigating the solubility of this compound highlights the intricate relationship between molecular structure and solvent properties, underscoring the importance of choosing the right environment for effective dissolution.

Interesting facts

Interesting Facts About (5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate

(5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate is an intriguing compound that captures the attention of both researchers and students alike. Here are some captivating aspects to consider:

  • Structural Complexity: This compound features a unique combination of a pyrazole ring and a carbamate group, leading to diverse reactivity and potential applications in various fields.
  • Potential Applications: The presence of the pyrazole moiety suggests potential use in pharmaceutical chemistry, particularly as a lead structure in the development of new therapeutic agents.
  • Mechanism of Action: Compounds like this often interact with biological systems at the enzyme level, showcasing their importance in drug design and medicinal chemistry.
  • Research Interest: Pyrazoles are known for their anti-inflammatory and analgesic properties, making this compound an exciting topic for further research to explore its pharmacological effects.
  • Scientific Collaboration: Its structure invites chemists to collaborate across disciplines, such as organic synthesis and computational chemistry, to investigate its properties and optimize its usability.

In summary, the complexity and potential applications of (5-methyl-2-phenyl-pyrazol-3-yl) N,N-dimethylcarbamate make it a compound of significant interest in the chemical sciences. As one breaks down its components, the interplay of structure and function unfolds, highlighting the essence of chemical innovation.

Synonyms
PYROLAN
Pyralan
87-47-8
Geigy G-22008
3-Methyl-1-phenylpyrazol-5-yl dimethylcarbamate
Caswell No. 574A
OMS 20
ENT 17,588
NSC 404297
Carbamic acid, dimethyl-, 3-methyl-1-phenyl-1H-pyrazol-5-yl ester
3-Methyl-1-phenylpyrazol-5-yl dimethyl carbamate
G 22008
G-22008
Dimethyl 5-(3-methyl-1-phenylpyrazolyl) carbamate
1-Phenyl-3-methyl-5-pyrazolyl N,N-dimethyl carbamate
Dimethylcarbamic acid, 3-methyl-1-phenylpyrazol-5-yl ester
EPA Pesticide Chemical Code 574200
1-phenyl-3-methyl-5-pyrazolyl dimethylcarbamate
BRN 0217907
AI3-17588
UNII-868K72C292
PYROLAN [MI]
Carbamic acid, dimethyl-, 3-methyl-1-phenylpyrazol-5-yl ester
Dimethylcarbamic acid 3-methyl-1-phenyl-1H-pyrazol-5-yl ester
Pyrazol-5-ol, 3-methyl-1-phenyl-, dimethyl carbamate (ester)
NSC-404297
(5-methyl-2-phenylpyrazol-3-yl) N,N-dimethylcarbamate
MLS000757184
868K72C292
DTXSID6042361
1-Fenyl-3-methyl-5-pyrazolylester kyseliny dimethylkarbaminove
3-methyl-1-phenyl-5-pyrazolyl dimethylcarbamate
1-Fenyl-3-methyl-5-pyrazolylester kyseliny dimethylkarbaminove [Czech]
3-Methyl-1-phenyl-5-pyrazolyl dimethyl carbamate
5-23-10-00530 (Beilstein Handbook Reference)
ENT-17588
dimethyl 5-(3-methyl-1-phenyl-pyrazolyl)carbamate
Pyrazol-5-ol, 3-methyl-1-phenyl-, dimethyl carbamate
Carbamic acid, dimethyl-, 5-methyl-2-phenyl-pyrazol-3-yl ester
N,N-DIMETHYLCARBAMIC ACID 3-METHYL-1-PHENYL-1H-PYRAZOL-5-YL ESTER
PYROLAN.
SCHEMBL499894
CHEMBL1610900
DTXCID4022361
HMS2886O15
AAA08747
NSC404297
AKOS040747322
WLN: T5NNJ AR& C1 EOVN1&1
NCGC00246807-01
Pyrazol-5-ol, dimethyl carbamate (ester)
SMR000529036
HY-129711
CS-0107596
NS00121575
Carbamic acid, 3-methyl-1-phenylpyrazol-5-yl ester
3-Methyl-1-phenyl-1H-pyrazol-5-yl dimethylcarbamate
Q27269716
3-Methyl-1-phenyl-1H-pyrazol-5-yl dimethylcarbamate #
Carbamic acid, 3-methyl-1-phenyl-1H-pyrazol-5-yl ester
DIMETHYL 5-(3-METHYL-1-PHENYLPYRAZOL) CARBAMATE
3-methyl-1-phenyl-1H-pyrazol-5-yl N,N-dimethylcarbamate
Carbamic acid, dimethyl-, 3-methyl-1-phenyl-1H-pyrazol-5-yl ester (9CI)