51069-90-0 Usage
Description
6-BROMO-4-CHLORO-3-FORMYLCOUMARIN 97, a coumarin derivative with the molecular formula C10H5BrClO3, is a chemical compound that incorporates bromine, chlorine, and a formyl group. It is recognized for its potential pharmacological and biological activities, making it a valuable component in the synthesis of pharmaceuticals and agrochemicals. Additionally, it serves as a fluorescent label for biological studies and contributes as a building block in organic synthesis, showcasing its versatility in chemistry and biology.
Uses
Used in Pharmaceutical and Agrochemical Industries:
6-BROMO-4-CHLORO-3-FORMYLCOUMARIN 97 is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, leveraging its potential pharmacological and biological properties to enhance the development of new therapeutic agents and crop protection products.
Used in Biological Research:
As a fluorescent label, 6-BROMO-4-CHLORO-3-FORMYLCOUMARIN 97 is utilized in various biological studies to track and visualize cellular processes, offering researchers a valuable tool for investigating complex biological phenomena.
Used in Organic Synthesis:
6-BROMO-4-CHLORO-3-FORMYLCOUMARIN 97 serves as a building block in organic synthesis, contributing to the creation of novel compounds with diverse applications across multiple fields, including materials science, medicinal chemistry, and more.
Check Digit Verification of cas no
The CAS Registry Mumber 51069-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,6 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51069-90:
(7*5)+(6*1)+(5*0)+(4*6)+(3*9)+(2*9)+(1*0)=110
110 % 10 = 0
So 51069-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H4BrClO3/c11-5-1-2-8-6(3-5)9(12)7(4-13)10(14)15-8/h1-4H
51069-90-0Relevant articles and documents
Synthesis and anti-inflammatory activity of 2-oxo-2H-chromenyl and 2H-chromenyl-5-oxo-2,5-dihydrofuran-3-carboxylates
Bhimapaka, China Raju,Karri, Shailaja,Kuncha, Madhusudana,Kurma, Siva Hariprasad,Sistla, Ramakrishna
, (2020/06/22)
Cycloaddition reaction of 4-chloro-2-oxo-2H-chromene-3-carbaldehydes (3a-g) and 4-chloro-2H-chromene-3-carbaldehydes (7a-h) with activated alkynes (4a-b) provided the 2-oxo-2H-chromenyl-5-oxo-2,5-dihydrofuran-3-carboxylates (5a-n) and 2H-chromenyl-5-oxo-2,5-dihydrofuran-3-carboxylates (8a-p). All the prepared compounds were screened for anti-inflammatory activity. In vitro anti-inflammatory activity data demonstrated that the compounds 5g, 5i, 5k-l and 8f are effective among the tested compounds against TNF-α (1.108 ± 0.002, 0.423 ± 0.022, 0.047 ± 0.001, 0.070 ± 0.002 and 0.142 ± 0.001 μM) in comparison with standard compound Prednisolone (0.033 ± 0.002 μM). Based on in vitro results, three compounds (5i, 5k and 8f) have been selected for in vivo experiments and these compounds are identified as better compounds with respect to anti-inflammatory activity in LPS induced mice model. Compound 5i was identified as potent and showed significant reduction in TNF-α and IL-6.