120595-88-2 Usage
Uses
Used in Pharmaceutical Industry:
(Phosphonooxy)cyclohexyl]oxy]phosphinyl]oxy]methyl]-1,2-ethanediyl ester is used as a key component in the development of drugs targeting various signaling pathways. Its unique structure allows it to interact with specific biological molecules, making it a promising candidate for the treatment of various diseases.
Used in Chemical Research:
In the field of chemical research, (phosphonooxy)cyclohexyl]oxy]phosphinyl]oxy]methyl]-1,2-ethanediyl ester serves as an important intermediate or building block for the synthesis of more complex molecules. Its versatile structure enables researchers to explore new chemical reactions and develop novel compounds with potential applications in various industries.
Used in Material Science:
(Phosphonooxy)cyclohexyl]oxy]phosphinyl]oxy]methyl]-1,2-ethanediyl ester can be utilized in the development of advanced materials with specific properties. Its unique structure can be exploited to create materials with enhanced performance in areas such as electronics, energy storage, and sensors.
Used in Signal Transduction Research:
As a critical component in signaling pathways, (phosphonooxy)cyclohexyl]oxy]phosphinyl]oxy]methyl]-1,2-ethanediyl ester is used in research to understand the complex mechanisms of cellular communication and regulation. This knowledge can be applied to develop targeted therapies for various diseases, including cancer and neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 120595-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,9 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 120595-88:
(8*1)+(7*2)+(6*0)+(5*5)+(4*9)+(3*5)+(2*8)+(1*8)=122
122 % 10 = 2
So 120595-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C41H81O19P3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(42)55-31-33(57-35(43)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)32-56-63(53,54)60-39-36(44)37(45)40(58-61(47,48)49)41(38(39)46)59-62(50,51)52/h33,36-41,44-46H,3-32H2,1-2H3,(H,53,54)(H2,47,48,49)(H2,50,51,52)/t33-,36-,37+,38+,39-,40-,41-/m1/s1
120595-88-2Relevant academic research and scientific papers
SYNTHESIS OF 1-O-(1,2-DI-O-PALMITOYL-SN-GLYCERO-3-PHOSPHO)-D-MYO-INOSITOL 4,5-BISPHOSPHATE: AN ANALOGUE OF NATURALLY OCCURING (Ptd)Ins(4,5)P2
Dreef, C. E.,Elie, C. J. J.,Hoogerhout, P.,Marel, G. A. van der,Boom, J. H. van
, p. 6513 - 6516 (2007/10/02)
Optically active 2,3,6-tri-O-benzyl-4,5-di-O-(trans-prop-1-enyl)-D-myo-inositol and 1,2-di-O-palmitoyl-sn-glycerol were coupled using mono- and bifunctional phosphitylating reagents to yield, after final removal of all benzyl-protecting groups the chiral title compound.
