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The chemical compound "w-3.4.5-Trimethoxy-benzoyl-4-3.4.5-trimethoxy-benzoyloxy-2-hydroxy-acetophenon" is a complex organic molecule with a molecular formula of C22H24O10. It features a benzoyl group (a benzene ring with a carbonyl group) at the 3, 4, and 5 positions, each substituted with a methoxy group (-OCH3). The compound also has a 2-hydroxy-acetophenon moiety, which is a phenol (a hydroxyl group attached to a benzene ring) with an acetophenone group (a methyl ketone attached to a benzene ring) at the 2-position. The entire structure is further connected by a benzoyloxy group, creating a complex ester linkage. w-3.4.5-Trimethoxy-benzoyl-4-3.4.5-trimethoxy-benzoyloxy-2-hydroxy-acetophenon is likely to be found in specialized chemical research or pharmaceutical applications due to its intricate structure and potential for specific interactions with biological systems.

22395-00-2

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22395-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22395-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,9 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22395-00:
(7*2)+(6*2)+(5*3)+(4*9)+(3*5)+(2*0)+(1*0)=92
92 % 10 = 2
So 22395-00-2 is a valid CAS Registry Number.

22395-00-2Relevant academic research and scientific papers

PHOTOACTIVABLE FLUOROPHORENES. 2. SYNTHESIS AND PHOTOACTIVATION OF FUNCTIONALIZED 3-AROYL-2-(2-FURYL)-CHROMONES

Cummings, Richard T.,DiZio, James P.,Krafft, Grant A.

, p. 69 - 72 (1988)

The synthesis and photochemistry of functionalized 3-aroyl-2-(2-furyl)-chromones 1 which are photoactivable fluorophores are described.Irradiation converts the non-fluorescent furyl chromones to highly fluorescent 1-arylfuro chromones 3.Functionality has been incorporated to permit covalent attachment, impart aqueous solubility and to maximize the fluorescence of the ultimate 1-arylfurochromone fluorophore.An efficient synthetic pathway to the furyl chromones via an intramolecular Dieckman cyclization also is described.

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