924265-80-5 Usage
Uses
Used in Organic Synthesis:
(R)-2-amino-2-(2,4,6-trimethylphenyl)ethanol is used as a chiral building block for the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable component in creating complex molecules with specific stereochemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (R)-2-amino-2-(2,4,6-trimethylphenyl)ethanol is used as a key intermediate in the synthesis of chiral pharmaceuticals. Its ability to influence the stereochemistry of the final product is crucial for the development of drugs with enhanced efficacy and selectivity.
Used in Anticancer Research:
(R)-2-amino-2-(2,4,6-trimethylphenyl)ethanol is studied for its potential as an anticancer agent. Its unique structure and functional groups may contribute to its ability to interact with biological targets, potentially leading to the development of novel cancer treatments.
Used in Anti-inflammatory Applications:
(R)-2-amino-2-(2,4,6-trimethylphenyl)ethanol is also being investigated for its potential anti-inflammatory properties. If proven effective, it could be used as a therapeutic agent in the treatment of various inflammatory conditions, providing an alternative to existing medications.
Check Digit Verification of cas no
The CAS Registry Mumber 924265-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,2,6 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 924265-80:
(8*9)+(7*2)+(6*4)+(5*2)+(4*6)+(3*5)+(2*8)+(1*0)=175
175 % 10 = 5
So 924265-80-5 is a valid CAS Registry Number.
924265-80-5Relevant academic research and scientific papers
Highly selective acetate aldol additions using mesityl-substituted chiral auxiliaries
Crimmins, Michael T.,Shamszad, Mariam
, p. 149 - 152 (2007/10/03)
(Chemical Equation Presented) Highly diastereoselective acetate aldol additions using chlorotitanium enolates of mesityl-substituted N-acetyloxazolidinethione and N-acetylthiazolidinethione auxiliaries are reported. These additions proceed in high yields
An effective and useful synthesis of enantiomerically enriched arylglycinols
Bandini, Marco,Cozzi, Pier Giorgio,Gazzano, Massimo,Umani-Ronchi, Achille
, p. 1937 - 1942 (2007/10/03)
A two-step synthesis of racemic arylglycinols, together with a simple and straightforward methodology for their resolution, is described. This method constitutes a practical means of preparing racemic and optically pure electron-rich or electron-poor subs
