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2,5-didecyloxy-1,4-bis(4-formylphenyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

850446-24-1

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850446-24-1 Usage

Chemical Structure

Consists of two benzene rings connected by a central carbon atom, with decyloxy and formyl groups attached.

Type

Bis(benzoylbenzene) derivative

Applications

Production of Liquid Crystal Materials: Used in electronic displays and devices.
Photosensitizer: Employed in organic electronics and optoelectronics.

Enhanced Properties

Solubility: Enhanced due to the presence of decyloxy groups.
Thermal Stability: Improved because of the decyloxy groups, making it suitable for various technological applications.

Versatility

Formyl Groups: Act as versatile building blocks for synthesizing other organic compounds, potentially useful in industrial and research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 850446-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,4,4 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 850446-24:
(8*8)+(7*5)+(6*0)+(5*4)+(4*4)+(3*6)+(2*2)+(1*4)=161
161 % 10 = 1
So 850446-24-1 is a valid CAS Registry Number.

850446-24-1Relevant academic research and scientific papers

Efficient synthesis of novel bis(dipyrromethanes) with versatile linkers via indium(III) chloride-catalyzed condensation of pyrrole and dialdehydes

Zhao, Hongbin,Liao, Junxu,Ning, Jingheng,Xie, Yujia,Cao, Yingjie,Chen, Liang,Yang, Deliang,Wang, Bangying

supporting information; experimental part, p. 3083 - 3088 (2011/02/22)

A new efficient and mild protocol for synthesizing a series of novel bis(dipyrromethanes) with versatile arylene linkers through an indi- um(III) chloride-catalyzed condensation reaction between various dialdehydes and pyrrole has been developed. This protocol is applicable to constructing a variety of bis(dipyrromethanes) with diverse functional linkers, which provides a powerful route to construct libraries of functionalized porphyrin dimers and even multiporphyrin arrays. Copyright

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