6338-89-2 Usage
Chemical structure
2-(4-chlorophenyl)-6-phenyl-4H-pyran-4-one is a chemical compound that consists of a 4H-pyran-4-one ring with a 4-chlorophenyl and a phenyl group attached to it.
Family
It belongs to the family of pyranones.
Anti-inflammatory properties
2-(4-chlorophenyl)-6-phenyl-4H-pyran-4-one has been shown to possess anti-inflammatory properties.
Antioxidant properties
The compound is also known for its antioxidant properties.
Antithrombotic properties
2-(4-chlorophenyl)-6-phenyl-4H-pyran-4-one has been shown to have antithrombotic properties.
Therapeutic applications
The compound has been studied for its potential therapeutic applications in the treatment of conditions such as ischemic heart disease, peripheral artery disease, and thrombotic disorders.
Anti-cancer properties
Cloricromene has shown potential as an anti-cancer agent and has been investigated for its effects on inhibiting tumor growth and metastasis.
Check Digit Verification of cas no
The CAS Registry Mumber 6338-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6338-89:
(6*6)+(5*3)+(4*3)+(3*8)+(2*8)+(1*9)=112
112 % 10 = 2
So 6338-89-2 is a valid CAS Registry Number.
6338-89-2Relevant articles and documents
Thermal addition reaction of aroylketene with 1-aryl-1- trimethylsilyloxyethylenes: Aromatic substituent effects of aroylketene and aryltrimethylsilyloxyethylene on their reactivity
Saitoh,Oyama,Sakurai,Niimura,Hinata,Horiguchi,Toda,Sano
, p. 956 - 966 (2007/10/03)
The thermal addition reaction of various aroylketenes (C) generated by the thermolysis of 5-aryldioxofurans (A) to 1-aryl-1-trimethylsilyloxyethylenes gave 1,5-diarylpentane-1,3,5-triones (D) and 2,6-diaryl-4H-pyran-4-ones (E). The introduction of electron withdrawing substituents in the aroylketene and of electron donating substituents facilitated the addition reaction. The observed substituent effects and the reaction mechanism are interpreted in terms of molecular orbital analyses.
Synthesis and Reactions of 3-Iodo-4H-pyran-4-ones
Marei, Mohamed Gaber,Mishrikey, Morcos Michael,El-Kholy, Ibrahim El-Sayed
, p. 1849 - 1852 (2007/10/02)
3-Iodo-4H-pyran-4-ones have been synthesized in excellent yield by the reaction of acetylenic β-diketones with iodine monochloride and were converted into the corresponding 4H-pyran-4-thiones.The iodopyrones and thiopyrones gave with methylamine the respe
