N-(4-Nitrobenzenesulfonyl)-3-formylvaline

Identification

Molecular formula

C₁₃H₁₄N₂O₇S

CAS number

104615-31-6

IUPAC name

3-formyl-2-[[(4-nitrophenyl)sulfonylamino]methyl]pentanoic acid

State

At room temperature, N-(4-Nitrobenzenesulfonyl)-3-formylvaline exists as a solid.

The compound is typically handled in a powder or crystalline form and does not easily transition to a liquid state except under specific laboratory conditions or processing steps.

Melting point (Celsius)

155.00

Melting point (Kelvin)

428.00

Boiling point (Celsius)

395.50

Boiling point (Kelvin)

668.50

General information

Molecular weight

340.34g/mol

Molar mass

340.3370g/mol

Density

1.5100g/cm³

Appearence

Appearance:

This compound appears as a crystalline solid. The exact color may vary, typically presenting as a white to off-white powder due to the presence of the nitro group, which can sometimes impart a light yellow tinge.

Comment on solubility

Solubility of 3-formyl-2-[[(4-nitrophenyl)sulfonylamino]methyl]pentanoic acid

The solubility characteristics of 3-formyl-2-[[(4-nitrophenyl)sulfonylamino]methyl]pentanoic acid (C₁₃H₁₄N₂O₇S) are intriguing due to its unique structure and functional groups. This compound contains multiple polar functional groups, which significantly influence its ability to dissolve in various solvents. Here are some key points to consider:

Polar Nature: The presence of sulfonamide and carboxylic acid groups contributes to its high polarity.
Hydrogen Bonding: The ability to form hydrogen bonds allows for increased solubility in polar solvents, such as water.
Solvent Dependence: It may exhibit solubility in organic solvents that can stabilize its polar regions, although the degree of solubility varies.
Experimental Data: Actual solubility values may vary based on pH and temperature conditions, and it is essential to refer to empirical studies for accurate measurements.

In summary, while the compound is likely to be soluble in polar solvents due to its functional groups, the degree of solubility will depend heavily on specific environmental factors. Understanding these variations is key in practical applications and further research.

Interesting facts

Interesting Facts about 3-Formyl-2-[[4-Nitrophenyl)sulfonylamino]methyl]pentanoic Acid

3-Formyl-2-[[4-nitrophenyl)sulfonylamino]methyl]pentanoic acid, a complex organic compound, is noteworthy for several reasons:

Unique Functional Groups: This compound features a variety of functional groups, including aldehyde, amine, and sulfonyl moieties, making it a fascinating candidate for studying chemical reactivity and interactions.
Biological Relevance: Compounds similar to this one are often investigated for their potential therapeutic applications, especially in the fields of medicinal chemistry and drug design.
Synthesis Challenges: The synthesis of this compound can present significant challenges due to the presence of multiple functional groups that can influence reactivity. This may require precise control of reaction conditions and techniques.
Electron-withdrawing Groups: The nitrophenyl group acts as an electron-withdrawing entity, which can significantly alter the electronic properties of the compound, impacting its interactions with biological targets.
Diverse Applications: Compounds in this class are often explored for their roles in developing new materials, dyes, or as intermediates in organic synthesis.

As a chemical entity, 3-formyl-2-[[4-nitrophenyl)sulfonylamino]methyl]pentanoic acid embodies the intersection of synthetic complexity and potential utility in scientific research. Its study not only contributes to the knowledge of complex organic molecules but also opens avenues for innovative applications in various fields.

Synonyms

PD036055