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N'-Isopropylbenzohydrazide

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Identification
Molecular formula
C10H14N2O
CAS number
5329-29-9
IUPAC name
N'-isopropylbenzohydrazide
State
State

At room temperature, N'-Isopropylbenzohydrazide is typically in a solid state, characterized by its crystalline texture.

Melting point (Celsius)
94.00
Melting point (Kelvin)
367.15
Boiling point (Celsius)
335.50
Boiling point (Kelvin)
608.65
General information
Molecular weight
178.24g/mol
Molar mass
178.2380g/mol
Density
1.0690g/cm3
Appearence
N'-Isopropylbenzohydrazide typically appears as a white to off-white crystalline solid. It is known for having a fairly simple crystalline structure.
Comment on solubility

Solubility of N'-isopropylbenzohydrazide

N'-isopropylbenzohydrazide, with the chemical formula C10H14N2O, presents a unique profile when it comes to solubility. This compound typically exhibits the following characteristics:

  • Solvent Interaction: It is generally more soluble in organic solvents such as ethanol and acetone compared to water.
  • Hydrogen Bonding: The presence of the hydrazide functional group allows it to engage in hydrogen bonding, improving solubility in polar solvents.
  • Temperature Influence: As with many organic compounds, solubility can increase with temperature; therefore, testing at elevated temperatures may yield better results.

While it may not dissolve readily in water, the solubility profile of N'-isopropylbenzohydrazide highlights the significance of solvent choice in chemical processes. Understanding these properties can be crucial for applications involving this compound.

Interesting facts

Interesting Facts About N'-isopropylbenzohydrazide

N'-isopropylbenzohydrazide is a fascinating compound that connects a myriad of chemical reactions and applications. Here are some intriguing aspects of this compound:

  • Chemical Structure: This compound features a hydrazide functional group, which is noteworthy due to its biological significance and versatility in synthetic chemistry.
  • Role in Synthesis: N'-isopropylbenzohydrazide is often used as a building block in organic synthesis, leading to the development of various pharmaceuticals and agrochemicals.
  • Research Application: Compounds containing hydrazide groups have been studied for their antioxidant and antimicrobial activities, making them important in medicinal chemistry.
  • Safety Considerations: Due to its reactivity, it’s important to handle N'-isopropylbenzohydrazide with care, as with many hydrazine-derived compounds, to prevent potential hazards.
  • Synthetic Challenges: The formation of hydrazides can pose synthetic challenges, often requiring stringent conditions and precise stoichiometry, making the study of their synthesis fascinating for chemists.

As the famous chemist and Nobel laureate Robert H. Grubbs once said, "There are opportunities to make things that have not been made before." N'-isopropylbenzohydrazide exemplifies this spirit of discovery and innovation in the field of chemistry.

In summary, N'-isopropylbenzohydrazide serves as a pivotal compound that not only enhances our understanding of hydrazides but also sparks further research in various chemical fields.

Synonyms
3408-21-7
BENZOIC ACID, 2-ISOPROPYLHYDRAZIDE
C00JE2LO5P
NSC 50993
P 1052
BRN 2047396
1-Benzoyl-2-isopropylhydrazine
Benzoic acid, 2-(1-methylethyl)hydrazide
NSC-50993
UNII-C00JE2LO5P
DTXSID90187677
N'-ISOPROPYLBENZOIC HYDRAZIDE
DTXCID50110168
N'-isopropylbenzohydrazide
Benzoicacid,2-(1-methylethyl)hydrazide
N'-propan-2-ylbenzohydrazide
SCHEMBL5394237
N'-(propan-2-yl)benzohydrazide
JEDFDJQCNTWWDS-UHFFFAOYSA-N
BDBM468581
benzoic acid N'-isopropyl-hydrazide
NSC50993
STK369986
AKOS005445359
NCGC00341755-01
US10807944, Compound RLS2-185
AB01334194-02
SR-03000003258
SR-03000003258-1