| Chemical Name: | Cyclohexane, (1-isocyanatoethyl)-, (S)- |
| CAS Number: | 93470-27-0 |
| Product Number: | AG003CFS(AGN-PC-0W3290) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | |
| Molecular Weight: |
(S)-(+)-1-Cyclohexylethylisocyanate is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organic chemistry. Due to its unique structure and reactivity, this compound serves as a key building block in the preparation of various complex organic molecules.One of the primary applications of (S)-(+)-1-Cyclohexylethylisocyanate is in the synthesis of chiral compounds. Its enantiopure nature allows for the selective formation of chirally pure products, making it an essential reagent in asymmetric synthesis. By incorporating this compound into a reaction, chemists can control the stereochemistry of the resulting molecules with high precision.Additionally, (S)-(+)-1-Cyclohexylethylisocyanate is utilized in the preparation of pharmaceutical intermediates and agrochemicals. Its ability to introduce the cyclohexylethyl moiety into target molecules makes it a valuable tool for the design and synthesis of bioactive compounds. Researchers rely on this compound to construct complex molecular structures with specific biological activities.Furthermore, (S)-(+)-1-Cyclohexylethylisocyanate plays a crucial role in material science, where it is employed in the development of functional materials such as polymers, surfactants, and coatings. By incorporating this compound into polymerization reactions or surface modifications, scientists can tailor the properties of materials to meet specific industrial or technological requirements.Overall, (S)-(+)-1-Cyclohexylethylisocyanate stands as a fundamental reagent in organic synthesis, enabling chemists to access diverse chemical space and create intricate molecular architectures with high stereochemical control. Its broad utility across various fields underscores its significance in advancing the frontiers of chemistry and material science.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
