127103-49-5 Usage
Uses
Used in Organic Synthesis:
(R,R)-(-)-(trans)-2,3-bis(α-hydroxydiphenylmethyl)-1,4-dioxaspiro-[4.4]nonane is used as a key intermediate in organic synthesis for the creation of various complex molecules. Its unique spiroketal structure and optical activity contribute to the synthesis of a wide range of chemical compounds with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (R,R)-(-)-(trans)-2,3-bis(α-hydroxydiphenylmethyl)-1,4-dioxaspiro-[4.4]nonane is utilized as a building block for the development of new drugs. Its specific stereochemistry and spiroketal structure make it an attractive candidate for the design and synthesis of innovative pharmaceuticals with potential therapeutic benefits.
Used in Chemical Research:
(R,R)-(-)-(trans)-2,3-bis(α-hydroxydiphenylmethyl)-1,4-dioxaspiro-[4.4]nonane is also employed in chemical research to study the properties and reactivity of spiroketal compounds. This research can lead to a better understanding of the compound's potential applications and the development of new methodologies for the synthesis of related structures.
Overall, (R,R)-(-)-(trans)-2,3-bis(α-hydroxydiphenylmethyl)-1,4-dioxaspiro-[4.4]nonane is a versatile compound with significant potential in various fields, including organic synthesis, pharmaceutical research, and chemical research. Its unique structure and properties make it a valuable asset for researchers and industry professionals in the development of new chemicals and drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 127103-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,0 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127103-49:
(8*1)+(7*2)+(6*7)+(5*1)+(4*0)+(3*3)+(2*4)+(1*9)=95
95 % 10 = 5
So 127103-49-5 is a valid CAS Registry Number.
127103-49-5Relevant academic research and scientific papers
Highly isotactic optically active methacrylate polymers by free radical cyclopolymerization
Zheng, Shiying,Sogah, Dotsevi Y.
, p. 15469 - 15485 (2007/10/03)
Isospecific free radical cyclopolymerization of tartrate-based monomers gives polymers with very high optical rotations. Circular dichroism and polarimetric measurements suggest the polymers are rigid and ordered. Their high resistance to solvolysis suggests potential applications in chiral chromatography.
