130675-14-8 Usage
Uses
Used in Organic Synthesis:
(2R,4R)-1-BENZYLOXY-4,8-DIMETHYL-4-VINYL-NONANE-2,8-DIOL is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure and functional groups allow for various chemical reactions, enabling the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
(2R,4R)-1-BENZYLOXY-4,8-DIMETHYL-4-VINYL-NONANE-2,8-DIOL is used as an intermediate in the synthesis of pharmaceutical compounds. Its chiral nature and functional groups make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Biochemistry:
(2R,4R)-1-BENZYLOXY-4,8-DIMETHYL-4-VINYL-NONANE-2,8-DIOL is used in biochemical research to study the interactions between molecules and biological systems. Its unique structure and functional groups allow for the investigation of various biological processes and the development of new bioactive compounds.
Further research and analysis are necessary to fully understand the properties and potential uses of (2R,4R)-1-BENZYLOXY-4,8-DIMETHYL-4-VINYL-NONANE-2,8-DIOL, as its applications in different industries may vary depending on its specific characteristics and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 130675-14-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,7 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130675-14:
(8*1)+(7*3)+(6*0)+(5*6)+(4*7)+(3*5)+(2*1)+(1*4)=108
108 % 10 = 8
So 130675-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O3/c1-5-20(4,13-9-12-19(2,3)22)14-18(21)16-23-15-17-10-7-6-8-11-17/h5-8,10-11,18,21-22H,1,9,12-16H2,2-4H3/t18-,20-/m1/s1
130675-14-8Relevant 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).
