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9,9-DiMethyl-9H-fluorene-2-carbonitrile is an organic compound that serves as a key intermediate in the synthesis of various organic compounds and materials.

890134-27-7

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890134-27-7 Usage

Uses

Used in Chemical Synthesis:
9,9-DiMethyl-9H-fluorene-2-carbonitrile is used as a precursor in the synthesis of fluorescent diketopyrrolopyrroles, which are important for the development of various applications.
Used in Inks and Colorants Industry:
9,9-DiMethyl-9H-fluorene-2-carbonitrile is used as a key component in the production of inks and colorants, providing vibrant colors and stability to the final products.
Used in Plastics and Coatings Industry:
9,9-DiMethyl-9H-fluorene-2-carbonitrile is used as a pigment in the manufacturing of pigmented plastics and coatings, contributing to their color and durability.
Used in Non-Impact Printing Material:
9,9-DiMethyl-9H-fluorene-2-carbonitrile is used in the development of non-impact printing materials, such as inkjet inks, ensuring high-quality prints and long-lasting colors.
Used in Color Filters:
9,9-DiMethyl-9H-fluorene-2-carbonitrile is used in the production of color filters, which are essential components in various display technologies, such as LCDs and OLEDs.
Used in Cosmetics Industry:
9,9-DiMethyl-9H-fluorene-2-carbonitrile is used as a colorant in the cosmetics industry, providing a wide range of shades and enhancing the visual appeal of cosmetic products.

Check Digit Verification of cas no

The CAS Registry Mumber 890134-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,1,3 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 890134-27:
(8*8)+(7*9)+(6*0)+(5*1)+(4*3)+(3*4)+(2*2)+(1*7)=167
167 % 10 = 7
So 890134-27-7 is a valid CAS Registry Number.

890134-27-7Downstream Products

890134-27-7Relevant academic research and scientific papers

Nickel-Catalyzed Cyanation of Aryl Halides and Hydrocyanation of Alkynes via C-CN Bond Cleavage and Cyano Transfer

Chen, Hui,Sun, Shuhao,Liu, Yahu A.,Liao, Xuebin

, p. 1397 - 1405 (2020/02/04)

We report nickel-catalyzed cyanation and hydrocyanation methods to prepare aryl nitriles and vinyl nitriles from aryl halides and alkynes, respectively. Using inexpensive and nontoxic 4-cyanopyridine N-oxide as the cyano shuttle, the methods provide an efficient approach to prepare aryl cyanides and vinyl nitriles under mild and operationally simple reaction conditions with a broad range of functional group tolerances. In hydrocyanation of alkynes, the method demonstrated good regioselectivity, producing predominantly E- or Z-alkenyl nitriles in a controlled manner and exclusively Markovnikov vinyl nitriles when internal diaryl alkynes and terminal alkynes were applied as the substrates, respectively. The preliminary mechanistic investigation indicated that the C-CN bond cleavage process is promoted by oxidative addition to the nickel(I) complex in the cyanation of aryl halides, and further studies via a series of deuterium exchange experiments indicated that water serves as the hydrogen source for the hydrocyanation of alkynes.

Fluorenyl tetrazole iridium complexes, and preparation method and application thereof

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Paragraph 0084; 0085, (2018/04/03)

The invention provides fluorenyl tetrazole iridium complexes, and a preparation method and application thereof. The structural formula of the fluorenyl tetrazole iridium complexes is as described in the specification. R1 in the structural formula is H or DPA, and R2 in the formula is CH3 or C6H13. The fluorenyl tetrazole iridium complexes are prepared from cyclometalated ligand, metal centers andthe auxiliary ligand picolinic acid. The fluorenyl tetrazole iridium complexes have long luminescence life, mild synthesis reaction conditions and good market application prospects.

Fluorescent diketopyrrolopyrroles

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Page/Page column 125, (2011/09/19)

The present invention relates to fluorescent diketopyrrolopyrroles of the formula (I), or (III), a process for their preparation and their use for the preparation of inks, colorants, pigmented plastics for coatings, non-impact-printing material, color filters, cosmetics, polymeric ink particles, toners, as fluorescent tracers, in color changing media, in solid dye lasers, EL lasers and electroluminescent devices. A luminescent device comprising a compound, or composition according to the present invention is high in the efficiency of electrical energy utilization and high in luminance.

Fluorescent Diketopyrrolopyrroles

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, (2008/12/08)

The present invention relates to fluorescent diketopyrrolopyrroles of the formula (I), or (III), a process for their preparation and their use for the preparation of inks, colorants, pigmented plastics for coatings, non-impact-printing material, color filters, cosmetics, polymeric ink particles, toners, as fluorescent tracers, in color changing media, in solid dye lasers, EL lasers and electroluminescent devices. A luminescent device comprising a compound, or composition according to the present invention is high in the efficiency of electrical energy utilisation and high in luminance.

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