1490-20-6 Usage
Description
(R)-1-[[(hexadecanoyl)oxy]methyl]-4-hydroxy-8-methyl-3,5-dioxa-8-aza-4-phosphanon-1-yl oleate P-oxide is a complex organic molecule characterized by its unique structure and the presence of multiple functional groups. It features a long chain hexadecanoyl group attached to a hydroxy, methyl, and phosphanon-1-yl oleate group, along with oxygen, nitrogen, and phosphorus atoms. The P-oxide group indicates that the compound has undergone oxidation, resulting in a phosphorus-oxygen bond. This intricate molecular composition suggests potential biological activity and reactivity, making it a candidate for various applications.
Uses
Used in Pharmaceutical Industry:
(R)-1-[[(hexadecanoyl)oxy]methyl]-4-hydroxy-8-methyl-3,5-dioxa-8-aza-4-phosphanon-1-yl oleate P-oxide is used as a potential pharmaceutical agent for its unique structure and functional groups. The presence of oxygen, nitrogen, and phosphorus atoms, along with the P-oxide group, may allow for specific interactions with biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Industry:
In the chemical industry, (R)-1-[[(hexadecanoyl)oxy]methyl]-4-hydroxy-8-methyl-3,5-dioxa-8-aza-4-phosphanon-1-yl oleate P-oxide can be utilized as a building block or intermediate in the synthesis of more complex molecules. Its unique structure and functional groups may enable the creation of novel compounds with specific properties and applications.
Used in Research and Development:
(R)-1-[[(hexadecanoyl)oxy]methyl]-4-hydroxy-8-methyl-3,5-dioxa-8-aza-4-phosphanon-1-yl oleate P-oxide serves as a valuable compound for research and development purposes. Its complex structure and potential reactivity make it an interesting subject for studying various chemical and biological interactions, which could lead to the discovery of new applications and insights into its properties.
Used in Material Science:
(R)-1-[[(hexadecanoyl)oxy]methyl]-4-hydroxy-8-methyl-3,5-dioxa-8-aza-4-phosphanon-1-yl oleate P-oxide may also find applications in the field of material science. Its unique molecular structure and functional groups could be exploited to develop new materials with specific properties, such as improved stability, reactivity, or biocompatibility.
Check Digit Verification of cas no
The CAS Registry Mumber 1490-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1490-20:
(6*1)+(5*4)+(4*9)+(3*0)+(2*2)+(1*0)=66
66 % 10 = 6
So 1490-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C41H80NO8P/c1-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-41(44)50-39(38-49-51(45,46)48-36-35-42(3)4)37-47-40(43)33-31-29-27-25-23-21-18-16-14-12-10-8-6-2/h19-20,39H,5-18,21-38H2,1-4H3,(H,45,46)/b20-19+
1490-20-6Relevant articles and documents
Synthesis of Benzophenone-Containing Analogues of Phosphatidylcholine
Wang, Pingzhen,Blank, David H.,Spencer, Thomas A.
, p. 2693 - 2702 (2007/10/03)
As part of a collaborative study of cellular efflux of cholesterol and phospholipids, photoactivable analogues 4-8 of phosphatidylcholine (PC) having benzophenone groups in the choline moiety and at the end of the C2 and C1 alkyl chains have been synthesized. The efficient preparation via Suzuki coupling of the appropriate long-chain benzophenone-containing carboxylic acid and alcohol and their incorporation by adaptation of known approaches into the acyl- and ether-linked PC analogues 6-8 are described. Development of a method for radiolabeling these PC analogues, via hydrogenation of a double bond in modified side chains, is also described.
