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CAS 212908-67-3|salicyloyl phytosphingosine
CAS 212908-67-3|salicyloyl phytosphingosine also known as salicyloyl phytosphingosine, is a unique compound that combines the properties of salicylic acid and phytosphingosine. Salicylic acid is a well-known ingredient in skincare products due to its ability to exfoliate the skin, unclog pores, and reduce inflammation.
Product Description
CAS 212908-67-3|salicyloyl phytosphingosine also known as salicyloyl phytosphingosine, is a unique compound that combines the properties of salicylic acid and phytosphingosine. Salicylic acid is a well-known ingredient in skincare products due to its ability to exfoliate the skin, unclog pores, and reduce inflammation. On the other hand, phytosphingosine is a natural lipid that helps restore and strengthen the skin’s natural barrier function. When these two ingredients are combined in salicyloyl phytosphingosine, it creates a powerful compound that not only exfoliates and reduces inflammation but also helps improve the overall health and resilience of the skin. This compound can be found in various skincare products and is particularly beneficial for individuals with acne-prone or sensitive skin.,
Product Name: | salicyloyl phytosphingosine |
Synonyms: | 2-hydroxy-N-[(2S,3S,4R)-1,3,4-trihydroxyoctadecan-2-yl]benzamide;SALICYLOYL PHYTOSPHINGOSINE, Water-Soluble Salicyloyl Phytosphingosine,Salicyloyl Phytosphingosine Nano-Liposome;Benzamide, N-[(1S,2S,3R)-2,3-dihydroxy-1-(hydroxymethyl)heptadecyl]-2-hydroxy-;SALICYLOYL PHYTOSPHINGOSINE |
CAS: | 212908-67-3 |
MF: | C25H43NO5 |
MW: | 437.61 |
EINECS: | 855-895-8 |
CAS 212908-67-3, also known as (R)-3-((tert-butoxycarbonyl)amino)-1-(2,4-difluorophenyl)butan-1-one, is a synthetic compound with a unique chemical structure and diverse applications. This compound belongs to the family of organic compounds known as keto acids and derivatives, which are crucial in various biochemical processes.
The IUPAC name for CAS 212908-67-3 gives a glimpse into its molecular structure, consisting of a butan-1-one backbone with a tert-butoxycarbonyl-amino group attached to the third carbon atom. Additionally, a 2,4-difluorophenyl group is linked to the first carbon atom, further enhancing its chemical complexity.
CAS 212908-67-3 has found utility in several fields, including pharmaceuticals and chemical research. Its chiral nature, indicated by the (R) configuration, makes it particularly valuable in the development of chiral drugs, which target specific receptors or enzymes in the body. The tert-butoxycarbonyl-amino group provides stability and protection during synthesis, enabling the compound to undergo further chemical reactions without unwanted side reactions.
Furthermore, the presence of the 2,4-difluorophenyl group imparts unique pharmacological properties to CAS 212908-67-3. Fluorine substitution is known to enhance the lipophilicity, metabolic stability, and bioavailability of compounds, making them more suitable for drug development. This attribute has attracted interest in exploring the potential therapeutic applications of CAS 212908-67-3 in various diseases, such as cancer, neurological disorders, and infectious diseases.
In addition to its pharmaceutical relevance, CAS 212908-67-3 serves as a valuable tool in chemical research. Its intricate structure and functional groups make it an ideal candidate for studying reaction mechanisms, molecular interactions, and structure-activity relationships. Researchers can manipulate and modify the compound to gain insights into its chemical behavior and explore its potential as a building block for synthesizing new compounds with desired properties.
To sum up, CAS 212908-67-3 is a synthetic compound with a complex molecular structure, holding promise in both pharmaceutical and chemical research. Its chiral nature, along with the tert-butoxycarbonyl-amino and 2,4-difluorophenyl groups, contributes to its diverse applications in drug development and chemical studies. Continued exploration of CAS 212908-67-3’s properties and potential may lead to significant advancements in various scientific disciplines.