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1-(4-bromophenyl)-4-phenylnaphthalene is a chemical compound that features a naphthalene core with a 4-bromophenyl group at position 1 and a phenyl group at position 4. It is recognized for its fluorescence properties and is widely utilized as an intermediate in organic synthesis.

1170321-08-0

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1170321-08-0 Usage

Uses

Used in Dye and Pigment Production:
1-(4-bromophenyl)-4-phenylnaphthalene is used as an intermediate in the production of dyes and pigments for its ability to contribute to the color and fluorescence properties of these materials.
Used in Organic Electronics:
1-(4-bromophenyl)-4-phenylnaphthalene is used as a component in the development of organic electronics due to its unique molecular structure and properties that can enhance the performance of electronic devices.
Used in Materials Science:
1-(4-bromophenyl)-4-phenylnaphthalene is used as a research compound in materials science to explore its potential in creating new materials with specific properties, leveraging its fluorescence and structural characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1170321-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,0,3,2 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1170321-08:
(9*1)+(8*1)+(7*7)+(6*0)+(5*3)+(4*2)+(3*1)+(2*0)+(1*8)=100
100 % 10 = 0
So 1170321-08-0 is a valid CAS Registry Number.

1170321-08-0Downstream Products

1170321-08-0Relevant articles and documents

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE

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Paragraph 0262; 0264; 0271-0272, (2021/08/20)

Provided is an organic electroluminescent element comprising a compound that is represented by formula (1) and having a more improved lifetime. (In the formula, X, R1-R8, R11-R17, R21-R30, L1, L2, n, and Ar1-Ar3 are as defined in the description.)

One-pot synthesis of 1,4-diarylnaphthalenes via a Wittig-Horner reaction/[4+2] cycloaddition/dehydrogenation sequence

Chen, Zhengbo,Shou, Wangge,Wang, Yanguang

experimental part, p. 1075 - 1080 (2009/12/03)

A one-pot synthesis of 1,4-diarylnaphthalenes from cinnamaldehydes, dimethyl benzylphosphonates, and benzenediazonium-2-carboxylate is described. The tandem process involves the Wittig-Horner reaction of the cinnamaldehyde with the benzylphosphonate, [4+2

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