688021-88-7 Usage
Description
(S)-SN-1,2-DIOCTANOYL-3-BENZYLGLYCEROL, with the chemical abstracts service number 688021-88-7, is a synthetic organic compound that plays a significant role in various chemical reactions and processes. Its unique structure, featuring a glycerol backbone esterified with two octanoyl groups and a benzyl group, endows it with specific properties that make it valuable in organic synthesis.
Uses
Used in Organic Synthesis:
(S)-SN-1,2-DIOCTANOYL-3-BENZYLGLYCEROL is used as a key intermediate in organic synthesis for the preparation of complex organic molecules and pharmaceutical compounds. Its unique structure allows for versatile chemical modifications, making it a valuable building block in the synthesis of various target molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-SN-1,2-DIOCTANOYL-3-BENZYLGLYCEROL is utilized as a precursor in the development of new drugs. Its ability to be modified and incorporated into larger molecular frameworks makes it a promising candidate for the creation of novel therapeutic agents with potential applications in treating various diseases.
Used in Cosmetics Industry:
(S)-SN-1,2-DIOCTANOYL-3-BENZYLGLYCEROL may also find applications in the cosmetics industry, where it can be used as an ingredient in the formulation of skincare and beauty products. Its unique properties could contribute to the development of innovative cosmetic products with enhanced efficacy and performance.
Used in Research and Development:
In the realm of research and development, (S)-SN-1,2-DIOCTANOYL-3-BENZYLGLYCEROL serves as a valuable tool for scientists and researchers. It can be employed in the study of various chemical reactions and mechanisms, as well as in the development of new synthetic methodologies and techniques.
Overall, (S)-SN-1,2-DIOCTANOYL-3-BENZYLGLYCEROL is a versatile compound with a wide range of applications across different industries, particularly in organic synthesis, pharmaceuticals, cosmetics, and research and development. Its unique structure and properties make it a valuable asset in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 688021-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,0,2 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 688021-88:
(8*6)+(7*8)+(6*8)+(5*0)+(4*2)+(3*1)+(2*8)+(1*8)=187
187 % 10 = 7
So 688021-88-7 is a valid CAS Registry Number.
688021-88-7Relevant articles and documents
A synthesis of dioctanoyl phosphatidylinositol
Elliott, Thomas S.,Nemeth, Joseph,Swain, Simon A.,Conway, Stuart J.
scheme or table, p. 2809 - 2813 (2010/03/30)
A synthesis of the naturally occurring enantiomer of phosphatidylinositol is reported. A resolution strategy, using camphor as a chiral auxiliary is employed to obtain the desired, enantiomerically pure, inositol derivative. Dioctanoyl lipid chains are appended to the molecule, which are shorter than the naturally occurring lipid chains, providing the molecule with enhanced water solubility.
Synthesis and pharmacological evaluation of second-generation phosphatidic acid derivatives as lysophosphatidic acid receptor ligands
Durgam, Gangadhar G.,Tsukahara, Ryoko,Makarova, Natalia,Walker, Michelle D.,Fujiwara, Yuko,Pigg, Kathryn R.,Baker, Daniel L.,Sardar, Vineet M.,Parrill, Abby L.,Tigyi, Gabor,Miller, Duane D.
, p. 633 - 640 (2007/10/03)
Short-chain phosphatidic acid derivatives, dioctanoyl glycerol pyrophosphate (DGPP 8:0, 1) and phosphatidic acid 8:0 (PA 8:0, 2), were previously identified as subtype-selective LPA1 and LPA3 receptor antagonists. Recently, we report
