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1,3,5-Trimethylpyrazole

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Identification
Molecular formula
C6H10N2
CAS number
14684-94-1
IUPAC name
1,3,5-trimethylpyrazole
State
State

This compound is typically in a liquid state at room temperature.

Melting point (Celsius)
-9.00
Melting point (Kelvin)
264.15
Boiling point (Celsius)
161.00
Boiling point (Kelvin)
434.15
General information
Molecular weight
110.17g/mol
Molar mass
110.1670g/mol
Density
0.9123g/cm3
Appearence

1,3,5-Trimethylpyrazole is a colorless liquid.

Comment on solubility

Solubility of 1,3,5-trimethylpyrazole

The solubility of 1,3,5-trimethylpyrazole (C7H10N2) exhibits unique characteristics due to its molecular structure. This compound is a derivative of pyrazole, contributing to its solubility properties in various solvents. Some noteworthy points regarding its solubility include:

  • Water Solubility: 1,3,5-trimethylpyrazole is typically considered to have low solubility in water. This is attributed to its hydrophobic methyl groups.
  • Organic Solvents: The compound shows better solubility in organic solvents such as ethanol, methanol, and acetone. These polar aprotic solvents facilitate dissolution due to their favorable interactions with the nitrogen atoms present in the molecule.
  • Temperature Dependence: The solubility can increase with temperature, which is a common trait for many organic compounds. As the temperature rises, kinetic energy allows for better interaction with the solvent molecules.

Overall, the solubility of 1,3,5-trimethylpyrazole highlights the *importance of both molecular structure and solvent choice*, making it a versatile compound in various chemical applications.

Interesting facts

Interesting Facts about 1,3,5-Trimethylpyrazole

1,3,5-trimethylpyrazole is an intriguing compound that has garnered attention in both academic and industrial settings. As a member of the pyrazole family, this compound showcases properties that merit discussion from various scientific perspectives.

1. Structure and Isomers

The unique structure of 1,3,5-trimethylpyrazole features three methyl groups attached to a pyrazole ring, specifically at the 1, 3, and 5 positions. This arrangement can influence the compound's reactivity and stability:

  • Stable intermediates in organic synthesis
  • Potential for various derivative compounds through substitution reactions

2. Role in Agriculture

One of the prominent applications of 1,3,5-trimethylpyrazole is in the field of agriculture. It serves as a key intermediate in the synthesis of various agrochemicals. For example:

  • It is used in the formulation of certain herbicides and fungicides.
  • Its chemical properties make it suitable for enhancing crop protection against pests.

3. Research and Synthesis

Researchers have developed several synthetic routes for producing 1,3,5-trimethylpyrazole, often emphasizing efficiency and yield. Some synthetic methods include:

  • Condensation reactions involving hydrazine derivatives.
  • One-pot multi-component reactions that streamline the process.

As noted in a research publication, "The ability to manipulate the electronic properties of pyrazoles allows chemists to design more effective agrochemical products."

4. Applications Beyond Agriculture

In addition to its agricultural roles, 1,3,5-trimethylpyrazole has shown potential in other areas:

  • It may be used as a building block in pharmaceutical chemistry.
  • Its derivatives are being explored for their electronic properties in materials science.

Overall, 1,3,5-trimethylpyrazole stands out as a versatile compound with significant implications for both scientific research and practical applications in various industries.

Synonyms
1,3,5-TRIMETHYLPYRAZOLE
1072-91-9
1H-Pyrazole, 1,3,5-trimethyl-
Pyrazole, 1,3,5-trimethyl-
UNII-63938V7Z82
63938V7Z82
DTXSID70147951
DTXCID5070442
626-960-6
hnoqafmobrwdkq-uhfffaoysa-n
1,3,5-Trimethyl-1H-pyrazole
MFCD00015536
1,3,5-Trimethyl-1H-pyrazole;
SCHEMBL147208
1,3,5-Trimethylpyrazole, 97%
CHEBI:195104
1,3,5-Trimethyl-1H-pyrazole #
ALBB-004448
BCP18636
HY-N7086
s5147
STK396612
AKOS002656998
AC-4834
CCG-266050
CS-W013666
DS-1495
PD088276
SY014296
DB-027318
T2724
EN300-35528
11B-132
Q27263586