Skip to main content

4-(2-Naphthylamino)phenol

ADVERTISEMENT
Identification
Molecular formula
C16H13NO
CAS number
1940-14-3
IUPAC name
4-(2-naphthylamino)phenol
State
State

At room temperature, 4-(2-Naphthylamino)phenol is typically in a solid state. It is often processed in specialized containers to avoid degradation due to air and light exposure, which could affect its stability.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
460.00
Boiling point (Kelvin)
733.15
General information
Molecular weight
219.28g/mol
Molar mass
219.2670g/mol
Density
1.2857g/cm3
Appearence

4-(2-Naphthylamino)phenol appears as a crystalline solid. It can vary in color but is often found in shades ranging from light tan to brown. This compound tends to darken upon exposure to air or light due to potential oxidation processes.

Comment on solubility

Solubility of 4-(2-naphthylamino)phenol

The solubility of 4-(2-naphthylamino)phenol in various solvents is an interesting subject to explore. Generally, the solubility of this compound can be influenced by several factors, including:

  • Polarity: As a moderately polar compound, it tends to dissolve better in polar solvents.
  • Temperature: Increasing temperature typically enhances solubility for many organic compounds, including this one.
  • pH of the solvent: The ionization of the compound can vary with pH, affecting solubility in aqueous solutions.

Overall, 4-(2-naphthylamino)phenol is known to have limited solubility in water, which makes organic solvents like ethanol, methanol, or dichloromethane more favorable for dissolving this compound. To summarize, here are some key points regarding the solubility:

  1. Partially soluble in organic solvents.
  2. Low solubility in water.
  3. Solubility increases with temperature elevation.

In conclusion, understanding the solubility behavior of 4-(2-naphthylamino)phenol is crucial for its applications in various chemical processes and formulations, such as in pharmaceuticals and dyes.

Interesting facts

Interesting Facts about 4-(2-naphthylamino)phenol

4-(2-naphthylamino)phenol, often referred to as an essential compound in the field of organic chemistry, has sparked considerable interest among researchers and industry professionals alike due to its unique properties and applications.

Key Features

  • Structural Elegance: This compound possesses a fascinating structure, featuring both naphthyl and phenol components, which contribute to interesting electronic and steric properties.
  • Versatile Applications: It is primarily utilized in the synthesis of dyes and pigments. Its unique structure allows it to be an intermediate in the creation of various organic substances.
  • Biological Relevance: There has been research indicating that compounds like 4-(2-naphthylamino)phenol can exhibit biological activity, making them potential candidates for pharmaceuticals, particularly in the area of anti-cancer research.

Prominent Characteristics

This compound stands out because of its interesting reactivity:

  • Amino Group Reactivity: The amino group attached to the naphthyl ring can participate in nucleophilic substitutions, paving the way for further chemical modifications.
  • Phenolic Hydroxyl Functionality: The hydroxyl group contributes to hydrogen bonding capability, impacting solubility and interactions in various environments.

Scientific Significance

In the words of a prominent chemist, "The study of derivatives like 4-(2-naphthylamino)phenol opens doors to new horizons in the realms of synthetic organic chemistry." As both a student and a researcher, one can appreciate how compounds of this nature provide a vital link between basic research and practical applications.

Exploring compounds like 4-(2-naphthylamino)phenol not only enhances our understanding of complex chemical reactivity but also sheds light on the intricate relationships between chemical structure and function.

Synonyms
93-45-8
4-(naphthalen-2-ylamino)phenol
4-(2-NAPHTHYLAMINO)PHENOL
p-Oxinozon
Phenol, 4-(2-naphthalenylamino)-
p-(2-Naphthylamino)phenol
p-Hydroxyneozon
p-Oxyneozone
p-Hydroxyneozone
N-(4-Hydroxyphenyl)-2-naphthylamine
p-Hydroxyphenyl-2-naphthylamine
4-(2-Naphthalenylamino)phenol
Phenol, p-(2-naphthylamino)-
4-[(naphthalen-2-yl)amino]phenol
CCRIS 6073
2-(4'-Hydroxyphenylamino)-Naphthalene
4-(2-Naftylamino)fenol
N-p-Hydroxyphenyl-2-naphthylamine
N-p-Hydroxyphenyl-beta-naphthylamine
EINECS 202-248-7
NSC 15372
BRN 1642793
PARAOXYNEOZONE
391R4KT1XJ
p-(.beta.-Naphthylamino)phenol
p-Hydroxyphenyl-.beta.-naphthylamine
4-Hydroxyphenyl-.beta.-naphthylamine
N-(p-Hydroxyphenyl)-2-naphthylamine
NSC-15372
NSC-21065
UNII-391R4KT1XJ
N-(p-Hydroxyphenyl)-.beta.-naphthylamine
MLS002638427
DTXSID8025701
Phenol, 4-(2-naphthylamino)-
3-13-00-01031 (Beilstein Handbook Reference)
NAPHTHYLAMINO)PHENOL, 4-(2-
N-(4-HYDROXYPHENYL)-2-NAPHTHYLAMINE, 97
WLN: L66J CMR DQ
p-(beta-Naphthylamino)phenol
p-Hydroxyphenyl-beta-naphthylamine
4-(2-Naftylamino)fenol [Czech]
4-Hydroxyphenyl-beta-naphthylamine
NSC21065
p-(2-naphthylamino) phenol
BIDD:GT0834
SCHEMBL593005
DTXCID305701
CHEMBL1699265
HMS3089F24
NSC15372
AKOS021984255
AS-61152
SMR001547908
DB-057402
CS-0330231
NS00039559
Q27890213