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2-(3,5-dimethylphenyl)-1H-indene-1,3(2H)-dione is a complex organic chemical compound with the molecular formula C17H14O2. It is characterized by a 1H-indene-1,3(2H)-dione core, which is a type of indene derivative with a dione functional group. The molecule features a 3,5-dimethylphenyl group attached to the 2-position of the indene, which consists of two methyl groups attached to the 3rd and 5th carbon atoms of the phenyl ring. 2-(3,5-dimethylphenyl)-1H-indene-1,3(2H)-dione is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions and can be used as an intermediate in the production of more complex molecules. The compound's properties, such as its solubility and stability, can be influenced by the presence of the dimethylphenyl group, making it a versatile building block in organic synthesis.

6549-64-0

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6549-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6549-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6549-64:
(6*6)+(5*5)+(4*4)+(3*9)+(2*6)+(1*4)=120
120 % 10 = 0
So 6549-64-0 is a valid CAS Registry Number.

6549-64-0Upstream product

6549-64-0Downstream Products

6549-64-0Relevant academic research and scientific papers

Palladium-catalyzed chemoselective synthesis of indane-1,3-dione derivatives via tert-butyl isocyanide insertion

Duan, Huaqing,Chen, Zhong,Han, Li,Feng, Yulin,Zhu, Yongming,Yang, Shilin

, p. 6782 - 6788 (2015)

A simple and efficient strategy for the synthesis of indane-1,3-dione derivatives through a palladium(0)-catalyzed reaction incorporating tert-butyl isocyanide has been developed. In addition, by applying this protocol as the key step, indenopyrazole derivatives can be easily synthesized in high yields in a one-pot procedure. This methodology is tolerant of a wide range of substrates and applicable to library synthesis.

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