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2,4-diphenyl-3-formyl-4H-chromene is an organic compound belonging to the class of chromenes, characterized by a benzene ring fused to a furan ring with two phenyl groups and a formyl group attached to the chromene ring structure. It is a formylated derivative of 4H-chromene, a type of heterocyclic compound. This chemical exhibits unique structural features and reactivity, making it a promising candidate for various applications in pharmaceuticals, materials science, and organic synthesis.

123394-22-9

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123394-22-9 Usage

Uses

Used in Pharmaceutical Industry:
2,4-diphenyl-3-formyl-4H-chromene is used as a pharmaceutical compound for its potential biological activities. Its unique structure and reactivity may contribute to the development of new drugs and therapeutic agents.
Used in Materials Science:
In the field of materials science, 2,4-diphenyl-3-formyl-4H-chromene is used as a building block for the synthesis of advanced materials with specific properties. Its structural features can be utilized to create novel materials with applications in various industries.
Used in Organic Synthesis:
2,4-diphenyl-3-formyl-4H-chromene serves as a valuable intermediate in organic synthesis, enabling the synthesis of more complex organic molecules. Its reactivity and structural features make it a useful component in the preparation of various organic compounds for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 123394-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,3,9 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123394-22:
(8*1)+(7*2)+(6*3)+(5*3)+(4*9)+(3*4)+(2*2)+(1*2)=109
109 % 10 = 9
So 123394-22-9 is a valid CAS Registry Number.

123394-22-9Relevant academic research and scientific papers

FORMYLATION AND AMINOALKYLATION OF 2,4-DIARYL-4H-CHROMENES

Koblic, A. V.,Suzdalev, K. F.

, p. 155 - 158 (2007/10/02)

Under the conditions of the Vilsmeier and Mannich reactions 4H-chromenes form the products from substitution at position 3.Under the influence of perchloric acid in acetic anhydride the 3-formylchromenes undergo cyclization to benzoindeno-pyryli

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