The product is (r)-2,3-cyclohexylideneglyceraldehyde with the CAS number 78008-36-3. It is supplied directly from the factory at the best price. This chemical compound has a specific molecular structure with a cyclohexylidene group attached to a glyceraldehyde moiety. The purity of our product is carefully controlled to meet high - quality standards, ensuring its reliability for various applications. The physical state of the product might vary depending on the storage conditions, but it is generally available in a form that is suitable for easy handling in laboratory or industrial settings.
(r)-2,3-cyclohexylideneglyceraldehyde has a wide range of uses in the chemical and pharmaceutical industries. In the field of organic synthesis, it serves as a valuable building block. It can be used to create more complex molecules through various chemical reactions such as condensation, addition, and substitution reactions. For example, it can participate in the formation of chiral compounds, which are crucial in the development of new drugs. Chiral drugs often have different biological activities depending on their enantiomeric forms, and our product can be used as a starting material to synthesize the desired enantiomer.
In the pharmaceutical industry, it may be involved in the synthesis of active pharmaceutical ingredients (APIs). By incorporating (r)-2,3-cyclohexylideneglyceraldehyde into the synthesis pathway, researchers can introduce specific functional groups and stereochemistry to achieve the desired pharmacological properties of the final drug product.
When using (r)-2,3-cyclohexylideneglyceraldehyde, it is important to follow standard laboratory or industrial safety procedures. Wear appropriate personal protective equipment, including gloves, goggles, and lab coats. Store the product in a cool, dry place away from direct sunlight and sources of ignition. Before use, carefully read the product label and safety data sheet (SDS) for detailed information on handling, storage, and disposal.
In a laboratory setting, accurately measure the required amount of the product using calibrated equipment. When carrying out chemical reactions, ensure that the reaction conditions such as temperature, pressure, and reaction time are carefully controlled according to the specific reaction protocol. After the reaction is completed, follow proper purification and isolation procedures to obtain the desired product.
Case Study 1: A pharmaceutical research company was working on developing a new anti - cancer drug. They used (r)-2,3-cyclohexylideneglyceraldehyde as a key intermediate in the synthesis of the active pharmaceutical ingredient. By incorporating this compound into their synthesis route, they were able to introduce a specific chiral center into the molecule. Through a series of well - designed reactions, they successfully synthesized the target compound with high enantiomeric purity. In pre - clinical trials, the drug showed promising anti - cancer activity, demonstrating the importance of our product in the drug development process.
Case Study 2: An organic chemistry research group was studying the synthesis of natural products. They employed (r)-2,3-cyclohexylideneglyceraldehyde to construct a complex carbon skeleton. By carefully controlling the reaction conditions and using a combination of different reagents, they were able to achieve a high - yield synthesis of the natural product analogue. This work not only advanced the field of natural product synthesis but also highlighted the versatility of our product in organic chemistry research.
If you have any questions or need further information about (r)-2,3-cyclohexylideneglyceraldehyde, please feel free to contact us. Our email is info@vivalr.com and our phone number is (86) 15866781826. We are committed to providing you with high - quality products and excellent customer service.
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