Interesting facts
Interesting Facts about Naphthalene-2-Carbaldehyde
Naphthalene-2-carbaldehyde, often referred to in the scientific community as a derivative of naphthalene, is a fascinating compound with multiple applications and properties. Here are some intriguing facts about this versatile aldehyde:
- Structure and Reactivity: One of its striking features is the presence of a carbonyl group (–CHO) attached to a naphthalene ring. This unique combination alters the reactivity of the compound, making it a valuable reactant in organic synthesis.
- Synthesis: Naphthalene-2-carbaldehyde can be synthesized through various methods, including formylation reactions. The process often employs reagents that facilitate the insertion of the formyl group into the naphthalene structure, showcasing the elegance of organic chemistry.
- Applications: This compound serves as a critical intermediate in the synthesis of dyes, fragrances, and pharmaceuticals. Its aromatic structure enhances its utility in diverse chemical reactions.
- Biological Activity: Studies have shown that naphthalene derivatives may exhibit biological activities, potentially leading to the discovery of new therapeutic agents. The compound is under investigation for its potential as a lead structure in drug development.
- Historical Significance: The study of naphthalene compounds dates back to the 19th century when chemists first isolated naphthalene from coal tar. Naphthalene-2-carbaldehyde continues to be of interest today, bridging the gap between traditional chemistry and modern applications.
In summary, naphthalene-2-carbaldehyde is more than just a simple aldehyde. Its unique properties and applications make it an essential compound in the world of organic chemistry. As researcher and educator David W. C. MacMillan once stated, “The beauty of chemistry lies in its ability to create new horizons.” Naphthalene-2-carbaldehyde exemplifies this statement through its multifaceted roles in both research and industry.
Synonyms
2-Naphthaldehyde
66-99-9
2-Naphthalenecarboxaldehyde
naphthalene-2-carbaldehyde
beta-Naphthaldehyde
2-Formylnaphthalene
beta-Formylnaphthalene
beta-Naphthylaldehyde
.beta.-Naphthaldehyde
.beta.-Formylnaphthalene
beta-Naphthylcarboxaldehyde
2-naphthalenealdehyde
.beta.-Naphthylcarboxaldehyde
.beta.-Naphthylaldehyde
NSC 8557
2-naphthylaldehyde
naphthalene-2-carboxaldehyde
EINECS 200-640-2
GZX30H50DE
BRN 0507750
CHEBI:52368
2-naphthylcarboxaldehyde
NSC-8557
MFCD00004094
UNII-GZX30H50DE
DTXSID6075352
4-07-00-01288 (Beilstein Handbook Reference)
2-Formylnaphthalene; 2-Naphthalenealdehyde
Naphth2aldehyde
2-naphtaldehyde
b-Naphthaldehyde
2-Napthaldehyde
naphthyl aldehyde
2-naphtoaldehyde
2-naphthal
betaNaphthaldehyde
2-naphthoaldehyde
2Formylnaphthalene
2-naphthalaldehyde
b-Formylnaphthalene
betaNaphthylaldehyde
ss--Naphthaldehyde
beta-naphthoaldehyde
betaFormylnaphthalene
naphthalene-2-aldehyde
2-naphthalenecarbaldehyde
betaNaphthylcarboxaldehyde
2Naphthalenecarboxaldehyde
2-naphthalencarboxaldehyde
Naphtalene-2-carbaldehyde
2-Naphthaldehyde, 98%
naphthalene-2 carbaldehyde
bmse000679
2-Naphathalenecarboxaldehyde
SCHEMBL51340
CHEMBL2289234
DTXCID7044687
NSC8557
Formylnaphthalene;2-Naphthaldehyde
2-Naphthalenecarboxaldehyde (9CI)
BCP26680
CS-D1121
HY-Y0075
AKOS000120509
AC-1415
FN08328
AS-14485
BP-12503
DB-021404
N0003
NS00041031
EN300-20918
F10988
Q27104792
F2191-0027
Z104484858
200-640-2
Solubility of Naphthalene-2-carbaldehyde (C11H8O)
Naphthalene-2-carbaldehyde, also known as 2-naphthaldehyde, exhibits particular solubility characteristics that make it an intriguing compound in the realm of organic chemistry.
Solubility Characteristics:
These solubility traits highlight the compound's versatility in various chemical environments, making it valuable for diverse applications, particularly in the synthesis of other compounds. As with many organic compounds, the ability of naphthalene-2-carbaldehyde to dissolve in different media can significantly influence its reactivity and the outcomes of reactions in which it participates.