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5-fluoro-1,2,3,4-tetraphenylnaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38382-43-3

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38382-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38382-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,8 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38382-43:
(7*3)+(6*8)+(5*3)+(4*8)+(3*2)+(2*4)+(1*3)=133
133 % 10 = 3
So 38382-43-3 is a valid CAS Registry Number.

38382-43-3Downstream Products

38382-43-3Relevant academic research and scientific papers

Room Temperature Decarboxylative and Oxidative [2+2+2] Annulation of Benzoic Acids with Alkynes Catalyzed by an Electron-Deficient Rhodium(III) Complex

Honjo, Yusaku,Shibata, Yu,Kudo, Eiji,Namba, Tomoya,Masutomi, Koji,Tanaka, Ken

, p. 317 - 321 (2018)

It has been established that an electron-deficient (η5-cyclopentadienyl)rhodium(III) [CpERhIII] complex is capable of catalyzing the decarboxylative and oxidative [2+2+2] annulation of benzoic acids with alkynes to produce substituted naphthalenes at room temperature. The appropriate choice of the additive and the solvent is crucial for this transformation. This catalyst system allowed use of oxygen as a terminal oxidant and broadened the substrate scope including both aromatic and aliphatic alkynes. In this catalysis, the electron deficient nature of the CpERhIII catalyst would cause the strong rhodium-π interaction, which accelerates the decarboxylation as well as the C?H bond cleavage.

Synthesis of Benzo-Fused Cyclic Compounds via Rhodium-Catalyzed Decarboxylative Coupling of Aromatic Carboxylic Acids with Alkynes

Inai, Yasuhito,Usuki, Yoshinosuke,Satoh, Tetsuya

supporting information, p. 3029 - 3036 (2021/04/15)

The decarboxylative coupling of diversely substituted benzoic acids with internal alkynes proceeds smoothly in the presence of a [RhCl(cod)] 2/1,2,3,4-tetraphenyl-1,3-cyclopentadiene catalyst system to selectively produce highly substituted nap

Synthesis of highly substituted acenes through rhodium-catalyzed oxidative coupling of arylboron reagents with alkynes

Fukutani, Tatsuya,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

scheme or table, p. 2867 - 2874 (2011/05/28)

The rhodium-catalyzed oxidative 1:2 coupling reactions of arylboronic acids or their esters with alkynes smoothly proceed to produce the corresponding annulated products. Of special note, highly substituted, readily soluble, and tractable anthracene and tetracene derivatives can be obtained selectively from 2-naphthyl- and 2-anthrylboron reagents, respectively.

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