65383-61-1 Usage
Description
6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE is a chemical compound with the molecular formula C12H17ClO4. It is characterized by the presence of two methoxy groups at the 6th and 7th positions, a dimethyl group at the 2nd and 2nd positions, and a chloro group at the 4th position on a chromanone ring. 6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE has potential applications in various fields due to its unique structural features and chemical properties.
Uses
Used in Agricultural Applications:
6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE is used as a chemical probe for studying the response of P. sojae zoospores to a wide range of compounds that have structural similarity to genistein and daidzein. This research can help in understanding the mode of action of these compounds and their potential use as biocontrol agents against plant pathogens.
Used in Pharmaceutical Research:
6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE can be used as a starting material for the synthesis of various pharmaceutical compounds with potential therapeutic applications. Its unique structural features make it a promising candidate for the development of new drugs targeting specific biological pathways.
Used in Chemical Synthesis:
6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE can be used as an intermediate in the synthesis of other organic compounds, such as flavonoids, which have a wide range of biological activities, including antioxidant, anti-inflammatory, and anticancer properties.
Used in Analytical Chemistry:
6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE can be used as a reference compound in analytical methods, such as high-performance liquid chromatography (HPLC) and mass spectrometry, for the identification and quantification of similar compounds in complex mixtures.
Check Digit Verification of cas no
The CAS Registry Mumber 65383-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,8 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65383-61:
(7*6)+(6*5)+(5*3)+(4*8)+(3*3)+(2*6)+(1*1)=141
141 % 10 = 1
So 65383-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O4/c1-13(2)7-9(14)8-5-11(15-3)12(16-4)6-10(8)17-13/h5-6H,7H2,1-4H3
65383-61-1Relevant articles and documents
β,β-DIMETHYLACRYLOPHENONES AND A CHROMANONE FROM NAMA HISPIDUM AND J. JOHNSTONII
Roitman, James N.,Wollenweber, Eckhard
, p. 936 - 938 (1993)
A β,β-dimethacrylophenone and the corresponding chromanone were isolated from the leaf resin of Nama hispidum.The leaf exudate of N. johnstonii contains another β,β-dimethacrylophenone as colouring matter.Key Word Index - Nama hispidum; N. johnstonii; Hydrophyllaceae; leaf resin; dimethacrylophenones; chromanone.
Intermolecular C-O addition of carboxylic acids to arynes: Synthesis of o-hydroxyaryl ketones, xanthones, 4-chromanones, and flavones
Dubrovskiy, Anton V.,Larock, Richard C.
, p. 2789 - 2798 (2013/03/29)
An efficient and simple route to biologically and pharmaceutically important o-hydroxyaryl ketones, xanthones, 4-chromanones, and flavones has been developed utilizing readily available carboxylic acids and commercially available o-(trimethylsilyl)aryl tr
Discovery of novel benzopyranyl tetracycles that act as inhibitors of osteoclastogenesis induced by receptor activator of NF-κB ligand
Zhu, Mingyan,Kim, Myung Hee,Lee, Sanghee,Bae, Su Jung,Kim, Seong Hwan,Park, Seung Bum
supporting information; experimental part, p. 8760 - 8764 (2011/02/23)
A novel benzopyran-fused molecular framework 7ai was discovered as a specific inhibitor of RANKL-induced osteoclastogenesis using a cell-based TRAP activity assay from drug-like small-molecule libraries constructed by diversity-oriented synthesis. Its inhibitory activity was confirmed by in vitro evaluations including specific inhibition of RANKL-induced ERK phosphorylation and NF-κB transcriptional activation. 7ai can serve as a specific small-molecule modulator for mechanistic studies of RANKL-induced osteoclast differentiation as well as a potential lead for the development of antiresorptive drugs.
