130129-22-5 Usage
Uses
Used in Pharmaceutical Synthesis:
(4S,6R)-6-BENZYLOXYMETHYL-4-METHYL-4-VINYL-TETRAHYDRO-PYRAN-2-ONE is used as a key intermediate in the synthesis of various pharmaceuticals and natural products. Its unique structure allows it to be a versatile building block for the development of new drugs and therapeutic agents.
Used in Chelating Applications:
(4S,6R)-6-BENZYLOXYMETHYL-4-METHYL-4-VINYL-TETRAHYDRO-PYRAN-2-ONE is used as a chelating ligand for binding and transporting metal ions. This property makes it useful in various applications, such as in the removal of heavy metals from the environment or in the development of metal-based catalysts.
Used in Medicine:
(4S,6R)-6-BENZYLOXYMETHYL-4-METHYL-4-VINYL-TETRAHYDRO-PYRAN-2-ONE has potential applications in the field of medicine, where it can be utilized in the development of new drugs or as a component of drug delivery systems.
Used in Biochemistry:
(4S,6R)-6-BENZYLOXYMETHYL-4-METHYL-4-VINYL-TETRAHYDRO-PYRAN-2-ONE can be used in biochemistry for studying the interactions between metal ions and biomolecules, as well as for the development of new biochemical assays and techniques.
Used in Materials Science:
(4S,6R)-6-BENZYLOXYMETHYL-4-METHYL-4-VINYL-TETRAHYDRO-PYRAN-2-ONE has potential applications in materials science, where it can be used to develop new materials with unique properties, such as metal-organic frameworks or advanced composites.
Check Digit Verification of cas no
The CAS Registry Mumber 130129-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130129-22:
(8*1)+(7*3)+(6*0)+(5*1)+(4*2)+(3*9)+(2*2)+(1*2)=75
75 % 10 = 5
So 130129-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H20O3/c1-3-16(2)9-14(19-15(17)10-16)12-18-11-13-7-5-4-6-8-13/h3-8,14H,1,9-12H2,2H3/t14-,16+/m1/s1
130129-22-5Relevant academic research and scientific papers
Enantiocontrolled synthesis of natural (+)-bakuchiol
Takano,Shimazaki,Ogasawara
, p. 3325 - 3326 (2007/10/02)
(+)-Bakuchiol (1), an irregular phenolic monoterpene of Psoralea corylifolia L., has been first synthesized in natural forms starting from (S)-O-benzylglycidol (2).
Enantio-and Stereo-controlled Construction of Tertiary and Quaternary Carbon Centers Using Chiral O-Benzylglycidol as Template
Takano, Seiichi,Shimazaki, Youichi,Moriya, Minoru,Ogasawara, Kunio
, p. 1177 - 1180 (2007/10/02)
An efficient method for the enantio- and stereo-controlled construction of tertiary and quaternary carbon centers in a highly functionalized system has been developed using chiral O-benzylglycidol as template.
