74347-29-8 Usage
Uses
Used in Organic Synthesis:
(8,8-dimethyl-8-azoniabicyclo[3.2.1]oct-3-yl) 3-hydroxy-2-phenyl-propanoate is used as an intermediate in the synthesis of various organic compounds due to its complex molecular structure and the presence of a quaternary nitrogen atom, which can be exploited for the creation of novel chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (8,8-dimethyl-8-azoniabicyclo[3.2.1]oct-3-yl) 3-hydroxy-2-phenyl-propanoate may serve as a building block for the development of new drugs. Its unique structural features could potentially be harnessed to design molecules with specific biological activities, targeting various medical conditions.
Used in Materials Science:
(8,8-dimethyl-8-azoniabicyclo[3.2.1]oct-3-yl) 3-hydroxy-2-phenyl-propanoate could be utilized in the field of materials science for the development of new materials with specialized properties. (8,8-dimethyl-8-azoniabicyclo[3.2.1]oct-3-yl) 3-hydroxy-2-phenyl-propanoate's structural characteristics might contribute to the creation of materials with enhanced performance in areas such as electronics, coatings, or polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 74347-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74347-29:
(7*7)+(6*4)+(5*3)+(4*4)+(3*7)+(2*2)+(1*9)=138
138 % 10 = 8
So 74347-29-8 is a valid CAS Registry Number.
74347-29-8Relevant academic research and scientific papers
Wang, Zhaokun,Zhang, Qiongwen,Luo, Linda,Sun, Tiemin,Guo, Xingjie
, p. 558 - 565 (2017)
Three kinds of sulfated β-cyclodextrin (S-β-CD), including a single isomer, heptakis-6-sulfato-β-cyclodextrin (HS-β-CD), degree of substitution (DS) of 7, which was synthesized in our laboratory and another two commercialized randomly substituted mixtures, a sulfated β-cyclodextrin with DS of 7 to 11, as well as a highly sulfated-β-cyclodextrin with DS of 12 to 15, were used for the enantioresolution of 12 drugs (the β-blockers, phenethylamines, and anticholinergic agents) in capillary electrophoresis. The enantioseparation under varying concentrations of S-β-CD and background electrolyte pH were systematically investigated and compared. Based on the experimental results, the effect of the nature of S-β-CD and analyte structure on the enantioseparation is discussed.
