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22082-98-0

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22082-98-0 Usage

Description

Naphthalene, 2-(4-chlorophenyl)-, also known as 1-chloro-2-(4-chlorophenyl) naphthalene, is a chemical compound belonging to the family of naphthalene derivatives. It is characterized by the presence of a naphthalene ring with a chlorophenyl group attached at the 2nd position. This versatile chemical is widely used in research and industry for various applications.

Uses

Used in Research Laboratories:
Naphthalene, 2-(4-chlorophenyl)is used as a building block for the synthesis of various organic compounds. Its unique structure allows for the formation of new chemical entities with potential applications in different fields.
Used in Pharmaceutical Industry:
Naphthalene, 2-(4-chlorophenyl)is utilized in the production of pharmaceuticals. Its chemical properties make it a valuable intermediate in the synthesis of drugs with therapeutic potential.
Used in Agrochemical Industry:
Naphthalene, 2-(4-chlorophenyl)is also employed in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used as an Insecticide:
Naphthalene, 2-(4-chlorophenyl)has been shown to exhibit insecticidal properties. It is used as an insecticide in some applications, helping to control and eliminate pests in various settings.

Check Digit Verification of cas no

The CAS Registry Mumber 22082-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22082-98:
(7*2)+(6*2)+(5*0)+(4*8)+(3*2)+(2*9)+(1*8)=90
90 % 10 = 0
So 22082-98-0 is a valid CAS Registry Number.

22082-98-0Relevant articles and documents

Diels-Alder reactions of 2′-hydroxychalcones with ortho-benzoquinodimethane: A new synthesis of 3-aryl-2-naphthyl 2-hydroxyphenyl ketones

Brito, Cristela M.,Pinto, Diana C. G. A.,Silva, Artur M. S.,Silva, Ana M. G.,Tome, Augusto C.,Cavaleiro, Jose A. S.

, p. 2558 - 2569 (2006)

Diels-Alder reactions of the 2′-hydroxychalcones 1a-e with oriho-benzoquinodimethane (3) yielded the 3-aryl-1,2,3,4-tetrahydro-2-naphthyl 2-hydroxyphenyl ketones 4a-e in good yields. The dehydrogenation of the cycloadducts 4a-e to 3-aryl-2-naphthyl 2-hydroxyphenyl ketones 5a-e was studied. Good results were obtained when DDQ was used as oxidant and microwave irradiation as energy source. Several benzoxanthone derivatives were also obtained as minor products. Structures of all new compounds were established by extensive NMR studies. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

PHOSPHORESCENT HOST COMPOSITION, ORGANIC OPTOELECTRONIC DIODE, AND DISPLAY DEVICE

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Paragraph 0171; 0173-0174; 0222; 0225-0226, (2021/04/17)

Provided are a composition for a phosphorescent host including a first host represented by Chemical Formula 1, a second host represented by a combination of Chemical Formula 2 and Chemical Formula 3; and an organic optoelectronic device including an anode and a cathode facing each other and an organic layer disposed between the anode and the cathode, wherein the organic layer includes an auxiliary layer including at least one of a hole injection layer, a hole transport layer, an electron injection layer, and an electron transport layer and a light emitting layer, and the light emitting layer includes a phosphorescent dopant having a maximum photoluminescence wavelength of 550 nm to 750 nm along with the composition, and a display device including the same. Details of Chemical Formulae 1 to 3 are the same as defined in the specification.

Organic Light Emitting Material and Organic Light Emitting Diode Having The Same

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Paragraph 0283-0286, (2021/11/02)

The present invention relates to a compound derivative for an organic electroluminescent device and an organic electroluminescent device using the same. The present invention relates to an aromatic compound including an indolocarbazolyl group and a spirobifluorenyl group, and more particularly, to an aromatic compound including an indolocarbazolyl group and a spirobifluorenyl group.

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