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Thiram

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Identification
Molecular formula
C6H12N2S4
CAS number
137-26-8
IUPAC name
1,3-benzothiazol-2-yl N,N-dimethylcarbamodithioate
State
State

Thiram is typically a solid at room temperature.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
329.00
Boiling point (Kelvin)
602.15
General information
Molecular weight
240.43g/mol
Molar mass
240.4260g/mol
Density
1.2900g/cm3
Appearence

Thiram appears as a yellow to amber-colored powder. It is often made available in the form of a crystalline solid or as wettable powders and granules.

Comment on solubility

Solubility of 1,3-benzothiazol-2-yl N,N-dimethylcarbamodithioate

The solubility of 1,3-benzothiazol-2-yl N,N-dimethylcarbamodithioate is influenced by several factors, including its molecular structure and the nature of the solvent. Here are some key points to consider:

  • Polar vs. Nonpolar Solvents: As a general rule, polar compounds tend to dissolve well in polar solvents, while nonpolar compounds prefer nonpolar solvents. The structure of this compound, featuring polar functional groups, suggests that it may exhibit some degree of solubility in polar solvents like water or alcohol.
  • Temperature Dependence: The solubility of chemical compounds often increases with temperature. Therefore, 1,3-benzothiazol-2-yl N,N-dimethylcarbamodithioate might become more soluble in hot solvents, which is an important consideration for practical applications.
  • pH Sensitivity: The solubility can also be affected by the pH of the solution. Compounds with acidic or basic groups may ionize in different pH environments, altering their solubility. For this compound, understanding its behavior in various pH levels can provide insights into its solubility profile.
  • Interactions with Solvent: The solubility may also be influenced by specific interactions such as hydrogen bonding or van der Waals forces between the solvent and the compound, which can enhance solubility in chosen media.

Overall, while specific solubility data may be limited, considering these factors can aid in predicting how 1,3-benzothiazol-2-yl N,N-dimethylcarbamodithioate behaves in different solvent systems. Experimentation and empirical studies will ultimately determine the precise solubility characteristics of this compound.

Interesting facts

Interesting Facts about 1,3-Benzothiazol-2-yl N,N-Dimethylcarbamodithioate

1,3-Benzothiazol-2-yl N,N-dimethylcarbamodithioate is a compound that belongs to the fascinating world of heterocyclic chemistry. Here are some engaging insights into this unique compound:

  • Dual Function: This compound is known for its roles as both a pesticide and a *fungicide*, making it particularly useful in agricultural practices.
  • Structural Significance: The inclusion of a benzothiazole ring in its structure not only provides distinct chemical properties but also enhances its biological activity, as benzothiazoles are often associated with *pharmacological effects*.
  • Complex Formation: The compound is capable of forming complexes with various metal ions, which can influence its efficacy as a pesticide and its behavior in various environmental conditions.
  • Research Focus: Scientists are excited about this compound due to ongoing studies exploring its potential in *medicinal chemistry*, where its derivatives could lead to new therapeutic agents.
  • Environmentally Relevant: Understanding how compounds like this behave in ecosystems is essential, especially related to *residue management* and *toxicity assessments* in agricultural settings.
  • Innovative Applications: Beyond agriculture, the compound may hold promise in materials science, with potential applications in the development of *novel coatings* and *polymers*.

In summary, 1,3-Benzothiazol-2-yl N,N-dimethylcarbamodithioate is more than just a chemical entity; it is a *bridge* between various fields of science, including chemistry, agriculture, and medicine, showcasing the interdisciplinary nature of modern research.

Synonyms
3432-25-5
2-Dimethyldithiocarbamyl benzothiazole
Benzothiazole, 2-dimethyldithiocarbamyl-
FOO2R88VZU
CARBAMIC ACID, DIMETHYLDITHIO-, 2-BENZOTHIAZOLYL ESTER
NSC 65288
2-Dimethyl dithiocarbamyl benzothiazole
BRN 0196369
Carbamodithioic acid, dimethyl-, 2-benzothiazolyl ester
UNII-FOO2R88VZU
NSC-65288
2-Benzothiazolyl N,N-dimethylcarbamodithioate
DTXSID00187885
4-27-00-01851 (Beilstein Handbook Reference)
CARBAMODITHIOIC ACID, N,N-DIMETHYL-, 2-BENZOTHIAZOLYL ESTER
DTXCID60110376
Carbamodithioic acid, dimethyl-, 2-benzothiazolyl ester (9CI)
USAF T-7
benzo[d]thiazol-2-yl dimethylcarbamodithioate
1,3-benzothiazol-2-yl N,N-dimethylcarbamodithioate
NCIOpen2_002896
SCHEMBL11167407
NSC65288