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(4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate

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Identification
Molecular formula
C20H16N2O5
CAS number
937032-44-3
IUPAC name
(4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate
State
State
At room temperature, (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate is a solid, typically found in a crystalline form.
Melting point (Celsius)
157.00
Melting point (Kelvin)
430.00
Boiling point (Celsius)
698.00
Boiling point (Kelvin)
971.15
General information
Molecular weight
348.36g/mol
Molar mass
348.3250g/mol
Density
1.3800g/cm3
Appearence

(4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate typically appears as a crystalline solid. The crystal structure can be intricate due to the aromatic rings, and the compound may exhibit a pale color depending on the specific conditions of crystallization and purity. It is soluble in various organic solvents but generally insoluble in water.

Comment on solubility

Solubility of (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate

The solubility of (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate can be quite intricate due to its structural characteristics. Several factors contribute to the solubility of this compound:

  • Molecular Structure: The presence of both nitro and benzyloxy functional groups can influence solubility in various solvents.
  • Polarity: While the nitro group is polar and can enhance hydrogen bonding, the benzyloxy group is relatively hydrophobic, potentially lowering overall solubility in water.
  • Temperature: Solubility often increases with temperature; thus, higher temperatures may facilitate greater dissolution.
  • Solvent Type: The choice of solvent plays a crucial role. This compound is likely more soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO) than in polar solvents like water.

In practical applications, it is essential to analyze the solubility properties to optimize the compound's use. "Understanding solubility is key to effective formulation"—a principle that rings true in various chemical processes.

In summary, the solubility of (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate can be influenced by its molecular characteristics, solvent choice, and operational conditions, making thorough assessment vital for effective applications.

Interesting facts

(4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate

(4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate is a fascinating compound that belongs to the class of carbamates, which are widely recognized for their diverse applications in chemistry, agriculture, and pharmaceuticals. Here are some interesting facts about this compound:

  • Versatile Applications: Carbamates are commonly used as pesticides and herbicides. The unique functional groups in (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate may provide specific biological activity, making it valuable in agrochemical development.
  • Stable Structure: The incorporation of both nitrophenyl and benzyloxy groups into its structure confers stability and can influence the compound's reactivity. Such modifications are often explored in medicinal chemistry for drug design.
  • Biological Interest: Compounds like this one are of interest in medicinal research, particularly due to their potential as enzyme inhibitors. Studying their interaction with biological targets can lead to the development of new therapeutic agents.
  • Synthesis Potential: The synthesis of (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate involves the reaction of specific reagents. This provides a great opportunity for students and chemists to explore techniques such as nucleophilic substitution and functional group manipulation.
  • Research Opportunities: Given the compound’s structural uniqueness, it offers rich avenues for further research in both organic synthesis and material science. Students and researchers are encouraged to explore its properties and potential applications.

In summary, (4-nitrophenyl) N-(4-benzyloxyphenyl)carbamate exemplifies how structural modifications can significantly influence the properties and applications of chemical compounds. Engaging with such compounds can foster a deeper understanding of the intricate relationships within chemistry.

Synonyms
p-Nitrophenyl p-benzyloxycarbanilate
6186-11-4
O-(p-Nitrophenyl)-N-(p-benzyloxyphenyl)-urethan
CARBANILIC ACID, p-BENZYLOXY-, (p-NITROPHENYL) ESTER
NSC 79251
BRN 2782621
WLN: WNR DOVMR CO1R
DTXSID10210835
NSC79251
NSC-79251
Carbanilic acid, (p-nitrophenyl) ester
(4-Nitrophenyl)n-[4-(phenylmethoxy)phenyl]carbamate