22082-98-0

Basic information

• Product Name: Naphthalene, 2-(4-chlorophenyl)-
• CAS NO: 22082-98-0
• Molecular Formula: C16H11Cl
• Molecular Weight: 238.716
• Mol File: 22082-98-0.mol
• Article Data: 30

Chemical Properties

• CAS DataBase Reference: Naphthalene, 2-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 2-(4-chlorophenyl)-(22082-98-0)
• EPA Substance Registry System: Naphthalene, 2-(4-chlorophenyl)-(22082-98-0)

Safety Data

• Hazardous Substances Data: 22082-98-0(Hazardous Substances Data)

Usage

General Description

Naphthalene, 2-(4-chlorophenyl)- is a chemical compound that belongs to the family of naphthalene derivatives. It is also known by its chemical name 1-chloro-2-(4-chlorophenyl) naphthalene. Naphthalene, 2-(4-chlorophenyl)- is commonly used in research laboratories as a building block for the synthesis of various organic compounds. It is also used in the production of pharmaceuticals and agrochemicals. Additionally, it has been shown to exhibit insecticidal properties and is used as an insecticide in some applications. Overall, Naphthalene, 2-(4-chlorophenyl)- is a versatile chemical with various industrial and research applications.

Upstream product

• 637-87-6 1-Chloro-4-iodobenzene 
• 627906-96-1 2-(2-naphthyl)-5,5-dimethyl-1,3,2-dioxaborinane 
• 32316-92-0 naphthalene-2-boronic acid 
• 61358-25-6 bis(4-tert-butylphenyl)iodonium hexafluorophosphate 
• 580-13-2 2-bromonaphthalene 
• 127567-54-8 (4-chlorophenyl)(naphthalen-2-yl)sulfane 
• 4783-69-1 2-(4-chlorophenoxy)pyridine 
• 21473-01-8 2-naphthalenylmagnesium bromide 
• 1679-18-1 4-Chlorophenylboronic acid 
• 573-57-9 1,4-dihydronaphthalene-1,4-epoxide 
• 1159-54-2 tri(4-chlorophenyl)phosphine 
• 612-55-5 2-iodonaphthalene 
• 106-39-8 bromochlorobenzene 
• 2632-70-4 di-p-chlorophenyl zinc 

Downstream Products

• 359653-43-3 2-(4-N,N-dimethylaminophenyl)naphthalene 
• 1092390-02-7 4,4,5,5-tetramethyl-2-(4-(naphthalen-2-yl)phenyl)-1,3,2-dioxaborolane 

Relevant articles and documents

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

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.

Arylketones as Aryl Donors in Palladium-Catalyzed Suzuki-Miyaura Couplings

Herein, we report the arylation, alkylation, and alkenylation of aryl ketones via a palladium-catalyzed Suzuki-Miyaura cross-coupling reaction. The use of the pyridine-oxazoline ligand is the key to the cleavage of the unstrained C-C bond. The late-stage arylation of aryl ketones derived from drugs and natural products demonstrated the synthetic utility of this protocol.

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

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.