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1H,3H-Furo[3,4-c]furan, 3,6-bis(diphenylmethylene)-1,6a-diethoxytetrahydro-1,4-diphenyl- is a complex organic compound characterized by its unique molecular structure. It features a furo[3,4-c]furan core, which is a type of furan with a fused benzene ring. The compound is further defined by the presence of two diphenylmethylene groups attached at the 3 and 6 positions, which contribute to its stability and reactivity. Additionally, it has a tetrahydro structure, indicating the presence of four hydrogen atoms in a cyclic structure, and two ethoxy groups at the 1 and 6a positions, which may influence its solubility and chemical properties. 1H,3H-Furo[3,4-c]furan, 3,6-bis(diphenylmethylene)-1,6a-diethoxytetrahydro-1,4-diphenyl- is likely to be of interest in the field of organic chemistry, potentially for its use in the synthesis of more complex molecules or for studying the properties of furan derivatives.

96547-90-9

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96547-90-9 Usage

Molecular structure

1H,3H-Furo[3,4-c]furan, 3,6-bis(diphenylmethylene)-1,6a-diethoxytetrahydro-1,4-diphenylis a complex organic compound with a fused ring structure, containing two furan rings and multiple phenyl groups, as well as ethoxy and methylene side chains.

Aromatic rings

The compound contains multiple aromatic rings, which contribute to its stability and potential applications in organic synthesis and medicinal chemistry.

Ether linkages

The presence of ethoxy groups in the compound provides ether linkages, which can be useful for the development of novel drugs or as a starting material for the synthesis of complex organic molecules.

Unique fused ring structure

The compound's unique structure, with two furan rings fused together, may have specific biological or pharmacological properties that could be explored for various applications.

Potential applications

Due to its unique structure and functional groups, 1H,3H-Furo[3,4-c]furan, 3,6-bis(diphenylmethylene)-1,6a-diethoxytetrahydro-1,4-diphenylexhibits potential for use in organic synthesis, medicinal chemistry, and the development of novel drugs.

Side chains

The presence of methylene side chains in the compound may influence its reactivity, solubility, and other physical properties, making it suitable for various chemical reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 96547-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,4 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96547-90:
(7*9)+(6*6)+(5*5)+(4*4)+(3*7)+(2*9)+(1*0)=179
179 % 10 = 9
So 96547-90-9 is a valid CAS Registry Number.

96547-90-9Downstream Products

96547-90-9Relevant academic research and scientific papers

NOVEL COPPER(I) CHLORIDE-ASSISTED COUPLING REACTION OF 1-CHLORO-1-ARYLOYL-3,3-DIARYLALLENE TO AFFORD 3,7-DIOXA-2,6-DIARYL-4,8-BIS(DIARYLMETHYLENE)BICYCLOOCTA-1,5-DIENE AND 1,1,4,4,-TETRAARYL-3,6-DIARYLOYLHEXA-1,2-DIENE-5-YNE, AND THERMAL CYCLIZATIO

Toda, Fumio,Yamamoto, Masataka,Tanaka, Koichi,Mak, Thomas C.W.

, p. 631 - 634 (2007/10/02)

A novel CuCl-assisted coupling reaction of 1-chloro-1-aryloyl-3,3-diarylallene (5) and two new thermal cyclization reactions of 1,1,4,4-tetraaryl-3,6-diaryloylhexa-1,2-diene-5-yne (7) are described.

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