Interesting facts
Interesting Facts about 4-Amino-2-methyl-naphthalen-1-ol
4-Amino-2-methyl-naphthalen-1-ol is a fascinating compound due to its unique structural features and versatile applications. Here are some key points to consider:
- Structure: This compound showcases a naphthalene backbone, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings. The presence of an amino group and a hydroxyl group significantly influences its reactivity.
- Chemical Reactivity: The hydroxyl (-OH) group in 4-amino-2-methyl-naphthalen-1-ol allows for hydrogen bonding, which can enhance solubility in polar solvents and facilitate various chemical reactions.
- Biological Activity: Compounds like 4-amino-2-methyl-naphthalen-1-ol are often studied for their potential pharmacological properties. Various derivatives of naphthalene have been found to exhibit antimicrobial and anti-inflammatory activities.
- Dye Applications: This compound can serve as a precursor to various dyes and pigments, owing to the fact that aromatic compounds are commonly used in dye manufacturing due to their stability and vivid colors.
- Research Significance: In materials science and organic chemistry, 4-amino-2-methyl-naphthalen-1-ol is often used in the synthesis of novel materials and as a building block for complex structures.
- Environmental Impact: Understanding compounds like this is crucial, as naphthalene derivatives can have significant environmental implications. Some are toxic, prompting researchers to explore safer alternatives in various applications.
In summary, 4-amino-2-methyl-naphthalen-1-ol is not just another compound; it represents a rich area of exploration in both synthetic chemistry and applied sciences. Its structural characteristics and potential uses make it an intriguing subject for further research.
Synonyms
Vitamin k5
4-Amino-2-methyl-1-naphthol
83-70-5
4-amino-2-methylnaphthalen-1-ol
Synkamin
Synkamin base
1-Naphthalenol, 4-amino-2-methyl-
2-Methyl-4-amino-1-naphthol
3-Methyl-4-hydroxy-1-naphthylamine
4-Amino-2-methyl-1-naphthalenol
1-Hydroxy-2-methyl-4-aminonaphthalene
2-Methyl-4-amino-1-hydroxynaphthalene
1-NAPHTHOL, 4-AMINO-2-METHYL-
UNII-KKP97T7O0X
KKP97T7O0X
BRN 2719282
Synkamin; Synkamin base
VITAMIN K5 BASE
4-Amino-2-methyl-1-naphthalenol, hydrochloride
VITAMIN K5 [MI]
89298-62-4
CHEMBL5191355
DTXSID3075042
3-13-00-01920 (Beilstein Handbook Reference)
4-Amino-2-methyl-1-hydroxynaphthalene
4-Hydroxy-3-methyl-1-naphthylammonium chloride
VitaminK5
1-Naphthol, 4-amino-2-methyl-, hydrochloride (8CI)
SCHEMBL318448
DTXCID6048337
CHEBI:195927
BCP09306
HY-B1814
BDBM50597708
AKOS006273533
4-Amino-2-methyl-1-naphthalenol, 9CI
4-AMINO-2-METHYL-1-NAPHTHOL HCI
DA-49693
CS-0013859
NS00006537
EN300-332177
Q27282311
Vitamin k5;1-hydroxy-2-methyl-4-aminonaphthalene;2-methyl-4-amino-1-hydroxynaphthalene;2-methyl-4-amino-1-naphthol;3-methyl-4-hydroxy-1-naphthylamine;4-Amino-2-methyl-1-naphthol
Solubility of 4-amino-2-methyl-naphthalen-1-ol
4-amino-2-methyl-naphthalen-1-ol, a compound featuring an amino group and a hydroxyl group, demonstrates notable solubility characteristics in various solvents. The solubility can be influenced by factors including pH, temperature, and the presence of other solutes.
Water Solubility
This compound exhibits **moderate solubility** in water due to the presence of the hydroxyl (-OH) group, which can engage in hydrogen bonding with water molecules. Key points to consider include:
Solubility in Organic Solvents
4-amino-2-methyl-naphthalen-1-ol tends to be more soluble in organic solvents such as ethanol, methanol, and acetone. This is due to:
In summary, the solubility of 4-amino-2-methyl-naphthalen-1-ol is a balance between its polar and non-polar characteristics. To quote, "Understanding the solubility of compounds is essential in both industrial applications and in biological systems," highlighting the importance of such properties in practical scenarios.