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Bensulfuron-methyl

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Identification
Molecular formula
C17H13N4O7S2
CAS number
83055-99-6
IUPAC name
1,3-dihydro-2lambda6,1,3-benzothiadiazole 2,2-dioxide
State
State

At room temperature, Bensulfuron-methyl is typically found as a solid, given its use as a herbicide it might be commercially available in powder or granule form.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
299.33g/mol
Molar mass
299.3300g/mol
Density
1.5596g/cm3
Appearence

Bensulfuron-methyl typically appears as an off-white to beige solid in its pure form, often marketed as a powder or granules for agricultural purposes. Being intended for use as a herbicide, it might also be found in formulated products which can alter its appearance slightly, based on processing and added ingredients.

Comment on solubility

Solubility of 1,3-Dihydro-2λ6,1,3-benzothiadiazole 2,2-dioxide

The solubility of 1,3-dihydro-2λ6,1,3-benzothiadiazole 2,2-dioxide can be quite complex and is influenced by various factors. Here are some key points to consider:

  • Polarity: The compound contains both polar and non-polar functional groups, which can lead to a moderate solubility in polar solvents like water and ethanol.
  • Temperature: Solubility often increases with temperature; thus, the compound may dissolve more readily when heated.
  • pH levels: Changes in pH can affect the solubility due to ionization, particularly in solutions where acidic or basic conditions can impact solubility.
  • Precipitation: Under certain conditions, this compound may tend to precipitate out of solution, leading to challenges in maintaining desired concentrations.

Based on its structure, **"1,3-dihydro-2λ6,1,3-benzothiadiazole 2,2-dioxide"** should be considered on a case-by-case basis regarding solubility. As noted, **“the dissolution behavior can vary significantly with environmental conditions.”** Understanding these nuances is essential for applications in both research and industrial contexts.

Interesting facts

Exploring 1,3-Dihydro-2λ6,1,3-benzothiadiazole 2,2-dioxide

1,3-Dihydro-2λ6,1,3-benzothiadiazole 2,2-dioxide is a fascinating compound that bridges the worlds of organic chemistry and materials science. Its unique structure arises from a fusion of benzene and thiadiazole rings, setting the stage for intriguing applications and properties.

Key Features

  • Versatile Applications: This compound has garnered attention in various fields, including:
    • Organic synthesis
    • Photovoltaic devices
    • Electrochemical sensors
  • Synthetic Utility: Known for its versatile reactivity, it serves as a valuable intermediate in the synthesis of more complex molecules.
  • Biological Activity: Research has indicated that derivatives of this compound exhibit promising biological activities, including potential antitumor effects.

Interestingly, the presence of the thiadiazole moiety contributes to its electron-rich characteristics, making it an essential component in the design of materials for electronic and photonic applications. Its distinct chemical structure allows for various substitutions, which can tailor its properties for specific uses. As noted in some literature, "the functionalization of 1,3-dihydro-2λ6,1,3-benzothiadiazole can significantly enhance its physical and chemical properties, paving the way for novel discoveries."

In summary, 1,3-dihydro-2λ6,1,3-benzothiadiazole 2,2-dioxide is more than just a chemical compound; it is a gateway to innovative research and applications that bridge multiple scientific disciplines. Its ongoing study promises to unravel further benefits and uses, captivating the curiosity of scientists and researchers worldwide.

Synonyms
1615-06-1
1H,3H-2,1,3-Benzothiadiazole 2,2-dioxide
1,3-Btdzd
2,1,3-Benzothiadiazole, 1,3-dihydro-, 2,2-dioxide
DTXSID10167158
DTXCID5089649
1,3-Dihydro-2,1,3-benzothiadiazole 2,2-dioxide
1,3-Dihydrobenzo[c][1,2,5]thiadiazole 2,2-dioxide
1,3-dihydro-2,1,3-benzothiadiazole-2,2-dione
1,3-dihydro-2lambda6,1,3-benzothiadiazole 2,2-dioxide
MFCD01860233
1,3-dihydro-2,1,3-benzothiadiazole-2,2-dioxide
CHEMBL25646
2,1,3-Benzothiadiazole,1,3-dihydro-,2,2-dioxide
1,3-dihydro-2lambda6,1,3-benzothiadiazole-2,2-dione
SCHEMBL2235632
BAA61506
AKOS001445190
CS-0447693
EN300-31319
G28499
1,3-Dihydrobenzo[1,2,5]thiadiazole 2,2-dioxide
1,3-dihydrobenzo[1,2,5]thiadiazole-2,2-dioxide
AK-830/25033012
1,3-dihydro-2|E?,1,3-benzothiadiazole-2,2-dione
1,3-Dihydrobenzo[c][1,2,5]thiadiazole2,2-dioxide
1,3-Dihydro-2,1,3-benzothiadiazole 2,2-dioxide #
Z321036532
1,?3-?Dihydro-2,?1,?3-?benzothiadiazole 2,?2-?dioxide