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890134-27-7

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890134-27-7 Usage

Description

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.

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 articles and documents

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.

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.

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