24382-97-6

Basic information

• Product Name: Naphthalene, 1-(4-chlorophenyl)-
• Synonyms: 1-(4-chloro-phenyl)-naphthalene;1-(4-Chlor-phenyl)-naphthalin
• CAS NO: 24382-97-6
• Molecular Formula: C16H11Cl
• Molecular Weight: 238.716
• Mol File: 24382-97-6.mol
• Article Data: 25

Chemical Properties

• Boiling Point: 151-155 °C(Press: 0.4 Torr)
• Density: 1.188±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Naphthalene, 1-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 1-(4-chlorophenyl)-(24382-97-6)
• EPA Substance Registry System: Naphthalene, 1-(4-chlorophenyl)-(24382-97-6)

Safety Data

• Hazardous Substances Data: 24382-97-6(Hazardous Substances Data)

Upstream product

• 6273-43-4 3,4-dihydro-1-(p-chlorophenyl)naphthalene 
• 154872-88-5 4-(4-chloro-phenyl)-naphthalene-1,2-dicarboxylic acid-anhydride 
• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 637-87-6 1-Chloro-4-iodobenzene 
• 873-73-4 4-n-chlorophenylacetylene 
• 122-78-1 phenylacetaldehyde 
• 90-11-9 1-Bromonaphthalene 
• 1679-18-1 4-Chlorophenylboronic acid 
• 22871-77-8 5,5-dimethyl-2-(naphthalen-1-yl)-1,3,2-dioxaborinane 
• 106-39-8 bromochlorobenzene 
• 13922-41-3 1-Naphthylboronic acid 
• 21700-74-3 (p-chlorophenyl)triethoxysilane 
• 96-09-3 styrene oxide 

Downstream Products

• 1028729-05-6 4,4,5,5-tetramethyl-2-(4-(naphthalen-1-yl)phenyl)-1,3,2-dioxaborolane 
• 897671-78-2 N-[4-(1-naphthalenyl)phenyl]-phenyl-4-amine 
• 69505-29-9 2,3-Dichloro-1-(4-chloro-phenyl)-naphthalene 
• 69505-31-3 2,4-Dichloro-1-(4-chloro-phenyl)-naphthalene 
• 27331-37-9 4-(naphthalen-1-yl)benzonitrile 

Relevant articles and documents

MeOTf-catalyzed formal [4?+?2] annulations of styrene oxides with alkynes leading to polysubstituted naphthalenes through sequential electrophilic cyclization/ring expansion

MeOTf-catalyzed formal [4 + 2] annulation of styrene oxides with alkynes to afford polysubstituted naphthalenes has been realized, which undergoes sequential electrophilic cyclization/ring expansion. A range of substrates were tolerated in the formation of naphthalene derivatives with high regioselectivity in satisfactory yields. The reaction could also be carried out on gram scale.

C(sp2)-C(sp2) Suzuki cross-coupling of arylammonium salts catalyzed by a stable Pd–NHC complex

We have developed the Suzuki-Miyaura cross-coupling of aryl ammonium salts via C–N bond activation catalyzed by an easily prepared and bench-stable palladium-N-heterocyclic carbene complex. The reaction proceeded well under mild conditions with phenylboronic acid, pinacol ester or anhydride and provided yields of products up to 97% with good functional group compatibility. The direct arylation of arylamine can be performed by a two-step one-pot process and the protocol can be performed on the gram scale.

Arylation of aryllithiums with: S-arylphenothiazinium ions for biaryl synthesis

Aryllithiums are one of the most common and important aryl nucleophiles; nevertheless, methods for arylation of aryllithums to produce biaryls have been limited. Herein, we report arylation of aryllithiums with S-arylphenothiazinium ions through selective