114417-34-4 Usage
Uses
Used in Pharmaceutical Research:
7-Bromo-2,3-dihydroquinolin-4(1H)-one is used as a research compound for the development of new pharmaceuticals. Its unique chemical structure and properties make it a promising candidate for the synthesis of novel drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 7-Bromo-2,3-dihydroquinolin-4(1H)-one serves as a valuable compound for studying the properties and reactions of quinoline and its derivatives. It can be used to explore various chemical reactions, such as substitution, addition, and condensation, to synthesize new compounds with potential applications in various industries.
Used in Drug Synthesis:
7-Bromo-2,3-dihydroquinolin-4(1H)-one is used as a key intermediate in the synthesis of various drugs, particularly those targeting central nervous system disorders, inflammation, and other conditions. Its unique structure allows for the development of new drug candidates with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In medicinal chemistry, 7-Bromo-2,3-dihydroquinolin-4(1H)-one is employed as a building block for the design and synthesis of new bioactive molecules. Its versatile chemical properties enable the creation of novel compounds with potential therapeutic benefits, such as improved pharmacokinetics, enhanced potency, and reduced side effects.
Used in Drug Discovery:
7-Bromo-2,3-dihydroquinolin-4(1H)-one plays a crucial role in drug discovery processes, where it is used to identify and optimize potential drug candidates. Its unique chemical properties allow researchers to explore various structural modifications and evaluate their impact on the compound's biological activity and safety profile.
Used in Chemical Synthesis:
7-Bromo-2,3-dihydroquinolin-4(1H)-one is used as a versatile synthetic building block in the preparation of various organic compounds. Its reactivity and functional groups enable the synthesis of a wide range of chemical products, including dyes, pigments, and other specialty chemicals.
Used in Analytical Chemistry:
In analytical chemistry, 7-Bromo-2,3-dihydroquinolin-4(1H)-one can be employed as a reference compound or a standard for the development and validation of analytical methods. Its unique properties and stability make it suitable for use in chromatographic, spectroscopic, and other analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 114417-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114417-34:
(8*1)+(7*1)+(6*4)+(5*4)+(4*1)+(3*7)+(2*3)+(1*4)=94
94 % 10 = 4
So 114417-34-4 is a valid CAS Registry Number.
114417-34-4Relevant articles and documents
BIARYL COMPOUNDS USEFUL FOR THE TREATMENT OF HUMAN DISEASES IN ONCOLOGY, NEUROLOGY AND IMMUNOLOGY
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Paragraph 0351, (2015/06/25)
The present invention provides compounds and compositions thereof which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same.
Chromanylurea compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor and uses thereof
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Page/Page column 55, (2008/06/13)
Compounds that are antagonists of the VR1 receptor, having formula (I) [image] or a pharmaceutically acceptable salt, prodrug, or salt of a prodrug thereof, wherein A1, A2, A3, A4, R7, R8, R9, X, Y, Z, L, n, and m, are as defined herein, and are useful in disorders prevented or ameliorated by inhibiting the VR1 receptor.
Structure-activity relationships of antimalarial indoloquinolines
Werbel, L. M.,Kesten, S. J.,Turner, W. R.
, p. 837 - 852 (2007/10/02)
Structure-activity relationships have been ascertained and chemical metodology developed for a series of antimalarial 3-chloroindoloquinoline-5-oxides.The basic side chain as well as the ring N-oxide are critical for antimalarial activity as is a bromine or chlorine in position 3.Substitution at positions 7,8,9,10 in not essential, although the most potent analog in our studies was the 8-nitro compound 4vv. indoloquinolines / antimalarial agents
