934980-79-7 Usage
Uses
Used in Organic Synthesis:
2-(3-bromophenyl)butanoic acid serves as a key intermediate in organic synthesis, facilitating the creation of a diverse range of pharmaceuticals, agrochemicals, and other organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of complex organic molecules.
Used in Research and Development:
In the realm of research and development, 2-(3-bromophenyl)butanoic acid plays a crucial role in the exploration and creation of new chemical compounds and materials. Its distinctive chemical properties provide a platform for scientists to investigate novel reactions and syntheses, potentially leading to breakthroughs in material science and related fields.
Used in Pharmaceutical Industry:
2-(3-bromophenyl)butanoic acid is utilized as a precursor in the development of pharmaceuticals. Its unique chemical structure may contribute to the design of new drugs with specific therapeutic effects. 2-(3-bromophenyl)butanoic acid's potential applications in medicine and pharmacology are currently being explored, with the aim of leveraging its properties to address unmet medical needs.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 2-(3-bromophenyl)butanoic acid is employed as a starting material for the synthesis of various agrochemicals. Its chemical versatility allows for the development of compounds with targeted effects on pests or crops, potentially enhancing agricultural productivity and crop protection strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 934980-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,9,8 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 934980-79:
(8*9)+(7*3)+(6*4)+(5*9)+(4*8)+(3*0)+(2*7)+(1*9)=217
217 % 10 = 7
So 934980-79-7 is a valid CAS Registry Number.
934980-79-7Relevant academic research and scientific papers
Discovery of 2-methylpyridine-based biaryl amides as γ-secretase modulators for the treatment of Alzheimer's disease
Chen, Jian Jeffrey,Qian, Wenyuan,Biswas, Kaustav,Yuan, Chester,Amegadzie, Albert,Liu, Qingyian,Nixey, Thomas,Zhu, Joe,Ncube, Mqhele,Rzasa, Robert M.,Chavez, Frank,Chen, Ning,Demorin, Frenel,Rumfelt, Shannon,Tegley, Christopher M.,Allen, Jennifer R.,Hitchcock, Stephen,Hungate, Randy,Bartberger, Michael D.,Zalameda, Leeanne,Liu, Yichin,McCarter, John D.,Zhang, Jianhua,Zhu, Li,Babu-Khan, Safura,Luo, Yi,Bradley, Jodi,Wen, Paul H.,Reid, Darren L.,Koegler, Frank,Dean Jr., Charles,Hickman, Dean,Correll, Tiffany L.,Williamson, Toni,Wood, Stephen
supporting information, p. 6447 - 6454 (2013/11/19)
γ-Secretase modulators (GSMs) are potentially disease-modifying treatments for Alzheimer's disease. They selectively lower pathogenic Aβ42 levels by shifting the enzyme cleavage sites without inhibiting γ-secretase activity, possibly avoiding known adverse effects observed with complete inhibition of the enzyme complex. A cell-based HTS effort identified the sulfonamide 1 as a GSM lead. Lead optimization studies identified compound 25 with improved cell potency, PKDM properties, and it lowered Aβ42 levels in the cerebrospinal fluid (CSF) of Sprague-Dawley rats following oral administration. Further optimization of 25 to improve cellular potency is described.
Oxime substituted tetrahydronaphthalene derivatives having retinoid and/or retinoid antagonist-like biological activity
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, (2008/06/13)
Compounds of the formula STR1 have retinoid-like or retinoid antagonist-like biological activity.
