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1H-furo[3,4-b]chromene-3,9-dione is a chemical compound with the molecular formula C11H6O4. It is a heterocyclic organic compound that features a furan ring fused to a chromene structure, which is a benzopyran. The compound is characterized by the presence of two carbonyl groups, one at position 3 and the other at position 9, which contribute to its reactivity and potential applications in various chemical processes. This specific structure may be of interest in the fields of organic synthesis, medicinal chemistry, and materials science, where it could be explored for its properties and potential uses in the development of new drugs, dyes, or other chemical products.

4940-40-3

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4940-40-3 Usage

Type of compound

Furochromone

Natural occurrence

Found in various plants, including certain fruits and vegetables

Biological activities

Potential as a photosensitizer in photodynamic therapy for cancer treatment

Drug development

Promising candidate for pharmacological research due to its potent inhibition of cytochrome P450 enzymes

Risks

Known for its phototoxic and photogenotoxic effects, which must be considered when using or studying the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 4940-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4940-40:
(6*4)+(5*9)+(4*4)+(3*0)+(2*4)+(1*0)=93
93 % 10 = 3
So 4940-40-3 is a valid CAS Registry Number.

4940-40-3Downstream Products

4940-40-3Relevant academic research and scientific papers

One-pot synthesis of pyrano[3,4-b]chromones from chromone-3-carbaldehyde

Panja, Suman Kalyan,Maiti, Sourav,Banerjee, Subhabrata,Bandyopadhyay, Chandrakanta

body text, p. 1909 - 1914 (2010/10/02)

3-Formylchromone reacts with cyclohexyl isocyanide to produce pyrano[3,4-b]chromone, which rearranges to 1-benzopyrano[2,3-c]pyridine when heated with HCl in ethanol. Georg Thieme Verlag Stuttgart.

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