612086-25-6

Basic information

• Product Name: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-phenyl-1-naphthalenyl)-
• CAS NO: 612086-25-6
• Molecular Formula: C22H23BO2
• Molecular Weight: 330.234
• Mol File: 612086-25-6.mol

Chemical Properties

• CAS DataBase Reference: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-phenyl-1-naphthalenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-phenyl-1-naphthalenyl)-(612086-25-6)
• EPA Substance Registry System: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-phenyl-1-naphthalenyl)-(612086-25-6)

Safety Data

• Hazardous Substances Data: 612086-25-6(Hazardous Substances Data)

Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 22082-93-5 1-bromo-2-phenylnaphthalene 
• 573-97-7 1-bromo-2-naphthol 
• 126613-08-9 trifluoromethanesulfonic acid 1-bromonaphthalen-2-yl ester 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 
• 108-86-1 bromobenzene 
• 59046-72-9 o-(phenylethynyl)benzaldehyde 
• 536-74-3 phenylacetylene 

Downstream Products

• 1416339-69-9 1-(4-methylphenyl)-2-phenylnaphthalene 
• 1416339-71-3 1-(4-t-butylphenyl)-2-phenylnaphthalene 
• 1439303-40-8 C₄₂H₂₇Cl 
• 612086-27-8 4-chloro-3-(2-phenyl-naphthalen-1-yl)pyridine 
• 1347741-49-4 C₄₆H₃₃BN₂ 
• 278600-44-5 (+/-)-diethyl-[3-(2-phenylnaphthalen-1-yl)pyridin-4-yl]amine 
• 612086-26-7 (+/-)-3-bromo-4-chloro-5-(2-phenylnaphthalen-1-yl)pyridine 

Relevant articles and documents

NOVEL ORGANIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

The present invention provides a novel stable benzo[a]naphtho[2,1-c]tetracene compound and an organic light-emitting device including the compound. Provided is an organic compound represented by Formula [1] described in Claim 1. In Formula [1], R1 to R16 each independently selected from a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, a cyano group, a diphenylamino group, a pyridyl group, and an aryl group.

Rhenium-catalyzed regioselective synthesis of 1,2-disubstituted naphthalenes

Rhenium-catalyzed coupling reaction of alkynes with phenylacetaldehyde dimethylacetal in the presence of H2O regioselectively afforded the corresponding 1,2-disubstituted naphthalenes.

PROCESS FOR THE PREPARATION OF ATROPISOMERIC ANALOGUES OF 4-AMINOPYRIDINE

The present invention relates to a process for the preparation of 3,4-disubstituted pyridines from commercially available starting materials. In particular, the invention relates to the process for the preparation for a compound of formula (I) wherein a c

Concise synthesis, preparative resolution, absolute configuration determination, and applications of an atropisomeric biaryl catalyst for asymmetric acylation

A new three-step synthesis and resolution of nucleophilic catalyst 1 suitable for large-scale preparation has been developed, and this catalyst has been shown to be effective for the kinetic resolution and asymmetric desymmetrization of a range of sec-alcohol substrates.