1078-30-4 Usage
Description
7-Quinolinecarboxylic acid is an organic compound with the chemical formula C10H6NO2. It is an off-white powder and is commonly utilized in the chemical and genetic engineering of selective ion channel-ligand interactions. This makes it a valuable compound in various scientific and industrial applications.
Uses
Used in Chemical and Genetic Engineering:
7-Quinolinecarboxylic acid is used as a reactant for the chemical and genetic engineering of selective ion channel-ligand interactions. Its role in this application is to facilitate the development of new compounds or modifications to existing ones that can specifically target and interact with ion channels, which are crucial for various cellular functions and signaling pathways.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 7-Quinolinecarboxylic acid is used as a building block for the synthesis of various drugs, particularly those targeting ion channels. Its ability to interact with these channels makes it a promising candidate for the development of medications that can treat a range of conditions, from neurological disorders to cardiovascular diseases.
Used in Research and Development:
7-Quinolinecarboxylic acid is also used in research and development, where it serves as a key component in the design and synthesis of novel compounds with potential therapeutic applications. Its unique properties allow scientists to explore new avenues in drug discovery and to better understand the mechanisms of action of various ion channel modulators.
Used in Material Science:
In the field of material science, 7-Quinolinecarboxylic acid can be used to develop new materials with specific properties, such as those that can selectively interact with ion channels. This can lead to the creation of advanced materials for use in sensors, drug delivery systems, and other applications where precise control over ion channel interactions is required.
Synthesis Reference(s)
Journal of the American Chemical Society, 68, p. 2721, 1946 DOI: 10.1021/ja01216a093
Check Digit Verification of cas no
The CAS Registry Mumber 1078-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1078-30:
(6*1)+(5*0)+(4*7)+(3*8)+(2*3)+(1*0)=64
64 % 10 = 4
So 1078-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO2/c12-10(13)8-4-3-7-2-1-5-11-9(7)6-8/h1-6H,(H,12,13)
1078-30-4Relevant articles and documents
Metal-Free Dehydrogenation of N-Heterocycles by Ternary h-BCN Nanosheets with Visible Light
Zheng, Meifang,Shi, Jiale,Yuan, Tao,Wang, Xinchen
, p. 5487 - 5491 (2018)
An efficient metal-free catalytic system has been developed based on hexagonal boron carbon nitride (h-BCN) nanosheets for the dehydrogenation of N-heterocycles with visible light; hydrogen gas is released in the process, and thus no proton acceptor is needed. This acceptorless dehydrogenation of hydroquinolines, hydroisoquinolines, and indolines to the corresponding aromatic N-heterocycles occurred in excellent yield under visible-light irradiation at ambient temperature. With h-BCN as the photocatalyst and water as the solvent, this environmentally benign protocol shows broad substitution tolerance and high efficiency.
Novel indolyl derivatives which are L-CPT1 inhibitors
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Page/Page column 27, (2010/11/26)
The invention is concerned with novel heterobicyclic derivatives of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, A, X and Y are as defined in the description and in the claims, as well as physiologically acceptable salts and esters thereof. These compounds inhibit L-CPT1 and can be used as medicaments.
