Page last updated: 2024-12-08

1-(1-naphthyl)ethyl isocyanate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

## 1-(1-Naphthyl)ethyl isocyanate: A Versatile Building Block in Research

1-(1-Naphthyl)ethyl isocyanate is a chemical compound that acts as a versatile building block in various research fields. It's a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and features an isocyanate functional group, making it highly reactive.

Here's a breakdown of its structure and importance:

**Structure:**

* **Naphthalene Core:** The molecule is built upon a naphthalene core, a planar system with two fused benzene rings. This provides a rigid structure with aromatic character.
* **Ethyl Substituent:** An ethyl group (CH2CH3) is attached to the naphthalene core. This introduces a flexible chain and a slightly hydrophobic character.
* **Isocyanate Group:** The isocyanate group (-N=C=O) is the crucial functional group responsible for the compound's reactivity. It readily undergoes nucleophilic addition reactions, making it ideal for synthetic applications.

**Importance in Research:**

1-(1-Naphthyl)ethyl isocyanate finds application in various research areas, including:

* **Organic Synthesis:** It serves as a valuable reagent for the synthesis of diverse organic compounds, particularly those containing carbamate functionalities. This is achieved by reacting the isocyanate group with various nucleophiles, such as alcohols, amines, and thiols.
* **Materials Science:** It's employed in the synthesis of polymers, particularly polyurethanes. Its structure contributes to the physical properties of the resulting polymers, including their mechanical strength, flexibility, and thermal stability.
* **Medicinal Chemistry:** This compound is used in the development of new drugs and pharmaceuticals. Its structure can be modified to target specific biological receptors and pathways, leading to the creation of potent therapeutic agents.
* **Bioconjugation:** It's utilized in the development of bioconjugates, which are formed by linking a molecule to a biological molecule. This technique allows for the targeted delivery of drugs or diagnostic agents to specific cells or tissues.
* **Analytical Chemistry:** It can be used as a reagent in analytical chemistry techniques like derivatization reactions, enhancing the detectability of analytes by improving their volatility or solubility.

**Note:** As with any chemical compound, 1-(1-Naphthyl)ethyl isocyanate should be handled with caution. It can be toxic and should be used in a properly equipped laboratory under appropriate safety measures.

In summary, 1-(1-Naphthyl)ethyl isocyanate is a versatile chemical compound that plays a significant role in various scientific disciplines, particularly in organic chemistry, materials science, and medicinal chemistry. Its unique structure and reactivity make it a valuable tool for researchers seeking to develop novel materials, drugs, and analytical methods.

1-(1-naphthyl)ethyl isocyanate: used for analysis of phenylpropanolamine in plasma [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID602753
SCHEMBL ID714591
MeSH IDM0153443

Synonyms (15)

Synonym
1-(1-naphthyl)ethyl isocyanate, 95%
1-(1-isocyanatoethyl)naphthalene
1-(1-naphthyl)ethyl isocyanate
A825859
FT-0642086
FT-0641480
FT-0605024
AKOS015910213
88442-63-1
1-(naphth-1-yl)ethylisocyanate
SCHEMBL714591
(r)-(-)-1-(1-naphthyl)ethylisocyanate
naphthalene, 1-(1-isocyanatoethyl)-
EN300-316044
SY101168

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" It has been applied to the determination of (+)- and (-)-sotalol in plasma from twelve subjects dosed with racemic sotalol."( Enantioselective analysis of sotalol in plasma by reversed-phase high-performance liquid chromatography using diastereomeric derivatives.
Baker, PV; Hooper, WD, 1995
)
0.29
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (12.50)18.7374
1990's7 (87.50)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other9 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]