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1,3,4-Triphenylfluoren-9-one is a complex organic compound characterized by its unique molecular structure, which consists of a fluoren-9-one core with three phenyl groups attached at positions 1, 3, and 4. 1,3,4-triphenylfluoren-9-one is known for its potential applications in various fields, including materials science and organic chemistry, due to its stable and rigid structure. It is often used as a building block for the synthesis of more complex molecules and has been studied for its photophysical properties, which can be relevant in the development of advanced materials and chemical sensors. The compound's chemical formula is C33H21O, reflecting its composition of carbon, hydrogen, and oxygen atoms. Its molecular weight is approximately 431.51 g/mol, and it is typically obtained as a white crystalline solid. The compound's chemical properties and reactivity can be influenced by the electronic effects of the phenyl groups, making it a subject of interest for researchers exploring the relationship between molecular structure and chemical behavior.

6583-78-4

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6583-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6583-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6583-78:
(6*6)+(5*5)+(4*8)+(3*3)+(2*7)+(1*8)=124
124 % 10 = 4
So 6583-78-4 is a valid CAS Registry Number.

6583-78-4Downstream Products

6583-78-4Relevant academic research and scientific papers

A Simple and Versatile Acetylene Equivalent in Diels-Alder Reactions

Kumar, Perumal Raja

, p. 509 - 510 (1989)

Allyl phenyl sulphone and cinnamyl p-tolyl sulphone underwent cycloaddition with tetraphenylcyclopentadienone, indanocyclone, 1,3-diphenylisobenzofuran, and tetraphenylcyclopentadiene to give the adducts with elimination of methyl phenyl sulphone and meth

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