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Atrazine

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Identification
Molecular formula
C8H14ClN5
CAS number
1912-24-9
IUPAC name
N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine
State
State

Atrazine is typically solid at room temperature.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
215.68g/mol
Molar mass
215.6840g/mol
Density
1.1870g/cm3
Appearence

Atrazine appears as a white crystalline solid.

Comment on solubility

Solubility of N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine

The solubility of N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine is an intriguing aspect due to its unique structural characteristics. This compound features a trifluoromethyl group, which is known for altering solubility properties. Understanding its solubility can involve several factors:

  • Polarity: The presence of the trifluoromethyl group typically increases the polarity of the molecule, potentially enhancing its solubility in polar solvents.
  • Hydrogen bonding: As a diamine, N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine can engage in hydrogen bonding, which may facilitate solubility in solvents that can also act as hydrogen bond donors.
  • Solvent effects: Its solubility can vary greatly depending on the choice of solvent. For example, it may exhibit greater solubility in organic solvents like dimethyl sulfoxide (DMSO) compared to water.

In summary, while detailed experimental data may be essential for practical applications, one may postulate that this compound's unique trifluoromethyl group and amine functionalities collectively influence its solubility, making it a worthy candidate for exploration in various chemical environments.

Interesting facts

Interesting Facts About N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine

N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine is a fascinating compound that sits at the intersection of organic chemistry and materials science. Known for its unique structure, this compound boasts several intriguing characteristics:

  • Fluorinated Features: The presence of the trifluoromethyl group enhances the compound's hydrophobicity and increases its thermal stability, making it ideal for various applications in extreme conditions.
  • Diverse Applications: This compound has potential uses in the field of agrochemicals as a herbicide, as well as in pharmaceuticals for drug development due to its ability to interact with biological systems effectively.
  • Versatile Reactivity: The triazine ring structure is known for its stability and reactivity, allowing for interesting chemical transformations that can lead to novel derivatives.
  • Synthetic Pathways: The synthesis of N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine involves sophisticated organic reactions, showcasing the complex yet rewarding nature of modern synthetic chemistry.

Moreover, triazines, in general, are crucial in the development of agricultural chemicals. As a researcher, it is essential to understand both their environmental impact and their biochemical properties. As you delve deeper into this compound, remember that:

"Chemistry is the study of matter, but I prefer to see it as the study of change." – Author Unknown

This quote resonates with the journey of understanding and manipulating compounds like N2-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine, as we explore how their structures can be altered for enhanced functionality and utility in real-world applications.

Synonyms
N-Phenyl-6-trifluoromethyl-[1,3,5]triazine-2,4-diamine
368-61-6
BAS 07529138
MLS001202459
CHEMBL1523197
SCHEMBL10016364
HMS2813E23
STK203621
STK852520
AKOS000627405
AKOS005629956
NCGC00245419-01
SMR000524112
Z57049318
[1,3,5]Triazine-2,4-diamine, N-phenyl-6-trifluoromethyl-
N-phenyl-6-(trifluoromethyl)-1,3,5-triazine-2,4-diamine
N-[4-amino-6-(trifluoromethyl)-1,3,5-triazin-2-yl]-N-phenylamine
(6Z)-6-(phenylimino)-4-(trifluoromethyl)-1,6-dihydro-1,3,5-triazin-2-amine