404354-76-3 Usage
Uses
Used in Pharmaceutical Industry:
Benzeneacetic acid, 4-butyl-alpha-methyl, (-alpha-S)(9CI) is utilized as a key building block for the synthesis of a variety of drugs and pharmaceutical compounds. Its unique structure and chiral properties make it a valuable component in the development of new medications with improved efficacy and selectivity.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Benzeneacetic acid, 4-butyl-alpha-methyl, (-alpha-S)(9CI) is employed as a starting material for the exploration of novel drug candidates. Its diverse biological activities and potential therapeutic effects have made it a promising subject for research aimed at discovering new treatments for various diseases and conditions.
Used in Drug Development:
Benzeneacetic acid, 4-butyl-alpha-methyl, (-alpha-S)(9CI) is leveraged in drug development processes to create innovative pharmaceuticals with enhanced properties. Its incorporation into drug molecules can lead to improved pharmacokinetics, such as better absorption, distribution, metabolism, and excretion, as well as increased safety and efficacy profiles.
Used in Pharmacological Studies:
Benzeneacetic acid, 4-butyl--alpha--methyl-, (-alpha-S)(9CI) is also used in pharmacological studies to investigate its potential applications in treating specific diseases and conditions. Researchers are exploring its interactions with biological targets and evaluating its efficacy in preclinical models to determine its suitability for further development as a therapeutic agent.
Check Digit Verification of cas no
The CAS Registry Mumber 404354-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,3,5 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 404354-76:
(8*4)+(7*0)+(6*4)+(5*3)+(4*5)+(3*4)+(2*7)+(1*6)=123
123 % 10 = 3
So 404354-76-3 is a valid CAS Registry Number.
404354-76-3Relevant academic research and scientific papers
Aoki, Yoshio,Shitara, Hiroaki,Hirose, Takuji,Nohira, Hiroyuki
, p. 2219 - 2222 (2001)
New chiral dopants for nematic liquid crystals were synthesized using optically active 2-phenylpropanoic acid derivatives. The magnitude of the helical twisting power (HTP) was largely influenced by the terminal group of the asymmetric frame and the core
