67029-84-9 Usage
General Description
6-Chloro-7-methylchromone is a chemical compound with the molecular formula C11H7ClO2. It is a chromone derivative with a chlorine atom at the 6 position and a methyl group at the 7 position. 6-CHLORO-7-METHYLCHROMONE has been studied for its potential pharmaceutical and biological activities, including its anti-inflammatory, antioxidant, and antimicrobial properties. It has also been investigated for its potential use in cancer research and as a potential drug candidate for various medical conditions. 6-Chloro-7-methylchromone is a versatile and important chemical compound with potential applications in various fields of research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 67029-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67029-84:
(7*6)+(6*7)+(5*0)+(4*2)+(3*9)+(2*8)+(1*4)=139
139 % 10 = 9
So 67029-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO2/c1-6-4-10-7(5-8(6)11)9(12)2-3-13-10/h4-5H,2-3H2,1H3
67029-84-9Relevant articles and documents
Substituent-Oriented Synthesis of Substituted Pyrazoles/Chromeno[3,2- c]pyrazoles via Sequential Reactions of Chromones/3-Chlorochromones and Tosylhydrazones
Dai, Tianzi,Li, Qunyi,Zhang, Xiaofei,Yang, Chunhao
, p. 5913 - 5921 (2019/05/10)
A facile and efficient synthetic strategy for the chemoselective synthesis of monocyclic/tricyclic-fused pyrazoles was developed, and it was oriented by different 3-position substituents (H or Cl) on the chromones. The reaction proceeded in a one-pot sequential way with a broad substrate scope and moderate to excellent yields.
2,3-Unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines
Iaroshenko, Viktor O.,Mkrtchyan, Satenik,Gevorgyan, Ashot,Miliutina, Mariia,Villinger, Alexander,Volochnyuk, Dmytro,Sosnovskikh, Vyacheslav Ya.,Langer, Peter
supporting information; experimental part, p. 890 - 894 (2012/02/02)
A divergent and regioselective approach to fused pyridines was developed through formal [3 + 3] cyclocondensations from simple 2,3-unsubstituted chromones or their enaminone precursors.
