955095-30-4 Usage
Uses
Used in Cosmetics Industry:
2,4-bis(docosyloxy)benzaldehyde is used as an ingredient in cosmetic formulations for its hydrophobic properties, which can contribute to the texture and stability of products. Its long carbon chains may also provide emollient effects, enhancing the skin feel and moisturizing capabilities of cosmetic products.
Used in Pharmaceutical Industry:
In pharmaceutical applications, 2,4-bis(docosyloxy)benzaldehyde is used as a precursor in the synthesis of complex molecules, potentially leading to the development of new drugs. Its aldehyde functional groups facilitate chemical reactions that can be harnessed to create a variety of pharmaceutical compounds.
Used in Materials Science:
2,4-bis(docosyloxy)benzaldehyde is employed in materials science as a component in the development of new materials with specific properties. Its high molecular weight and hydrophobic nature may be utilized to create materials with tailored characteristics for various applications, such as in coatings, adhesives, or polymers.
Used in Chemical Synthesis:
As a chemical compound with aldehyde functional groups, 2,4-bis(docosyloxy)benzaldehyde is used as a building block in the synthesis of more complex organic molecules. Its reactivity in organic reactions makes it a valuable intermediate in the production of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 955095-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,5,0,9 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 955095-30:
(8*9)+(7*5)+(6*5)+(5*0)+(4*9)+(3*5)+(2*3)+(1*0)=194
194 % 10 = 4
So 955095-30-4 is a valid CAS Registry Number.
955095-30-4Relevant academic research and scientific papers
PRODUCTION METHOD OF OLIGONUCLEOTIDE
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, (2012/12/13)
The problem of the present invention is provision of a method of producing an n+p-mer oligonucleotide efficiently in a high yield, which includes use of, as a starting material, an n-mer oligonucleotide wherein the 3′-terminal hydroxyl group is protected,
REAGENT FOR ORGANIC SYNTHESIS AND METHOD OF ORGANIC SYNTHESIS REACTION WITH THE REAGENT
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Page/Page column 17, (2009/01/24)
A reagent for organic synthesis with which a chemical reaction can be conducted in a liquid phase and unnecessary compound(s) can be easily separated at low cost from the liquid phase after completion of the reaction. The reagent for organic synthesis reversibly changes from a liquid-phase state to a solid-phase state with changes in solution composition and/or solution temperature, and is for use in organic synthesis reactions. This reagent for organic syntheses facilitates process development. With the reagent, research on and development of, e.g., medicines through, e.g., compound library synthesis, etc. can be accelerated. It can hence contribute to technical innovations in the biochemical industry and chemical industry.
