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2-(Diisopentylamino)acetohydrazide

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Identification
Molecular formula
C12H26N2O
CAS number
14549-69-4
IUPAC name
2-(diisopentylamino)acetohydrazide
State
State

At room temperature, 2-(Diisopentylamino)acetohydrazide is typically a liquid or an oily substance.

Melting point (Celsius)
16.00
Melting point (Kelvin)
289.15
Boiling point (Celsius)
331.50
Boiling point (Kelvin)
604.65
General information
Molecular weight
215.35g/mol
Molar mass
215.3480g/mol
Density
0.9202g/cm3
Appearence

2-(Diisopentylamino)acetohydrazide appears as a colorless or pale yellow liquid. It may also appear as a light viscous oil due to its amine functional groups.

Comment on solubility

Solubility of 2-(diisopentylamino)acetohydrazide

2-(diisopentylamino)acetohydrazide is a compound that exhibits unique solubility characteristics due to its structural components. When evaluating its solubility, several important factors come into play:

  • Polarity: The presence of amino groups tends to enhance its solubility in polar solvents.
  • Hydrophobic Interactions: The diisopentyl groups impart hydrophobic characteristics, which can decrease solubility in water.
  • Solvent Type: This compound is likely to be more soluble in organic solvents such as ethanol, methanol, or DMSO, where hydrophobic interactions are less of a constraint.

As a general rule, one might find that:

  1. Higher temperatures can improve solubility for some compounds.
  2. pH levels in solution may also play a crucial role in altering the solubility due to ionization effects.

In conclusion, while 2-(diisopentylamino)acetohydrazide demonstrates limited solubility in water, it showcases better solubility in various organic solvents. Therefore, careful consideration of the solvent environment is essential when working with this compound.

Interesting facts

Interesting Facts about 2-(Diisopentylamino)acetohydrazide

2-(Diisopentylamino)acetohydrazide is a fascinating compound that straddles the realms of organic synthesis and medicinal chemistry. Its unique structure and functional groups make it a subject of interest for researchers and students alike. Here are some noteworthy aspects of this chemical:

  • Versatile Applications: This compound is often explored for its potential applications in pharmaceuticals, where it may be used as an intermediate in synthesizing various bioactive molecules.
  • Hydrazine Derivative: As a hydrazide, it exhibits interesting reactivity patterns, allowing it to participate in a variety of reactions such as acylation and condensation, which are crucial for drug discovery.
  • Study of Structure-Activity Relationships: Researchers analyze compounds like 2-(Diisopentylamino)acetohydrazide to better understand how structural modifications influence biological activity, paving the way for the design of more effective therapeutics.
  • Significance in Material Science: Beyond its biological applications, this compound can also play a role in the development of new materials due to its potential to form stable complexes with metals.

In the words of a renowned chemist, "The beauty of chemistry lies in its ability to transform simple substances into complex structures with immense potential." This sentiment resonates particularly well with compounds like 2-(Diisopentylamino)acetohydrazide, underscoring its importance in the broader field of chemical research.

As a scientist or chemistry student, delving deeper into the properties and reactions of this compound can unveil new opportunities that could lead to innovative solutions in health and industry.

Synonyms
N,N-Diisopentylglycine hydrazide
GLYCINE, N,N-DIISOPENTYL-, HYDRAZIDE
BRN 1210957
2644-39-5
DTXSID70181037
DTXCID80103528