1416371-19-1

Basic information

• Product Name: 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane
• Synonyms: 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane
• CAS NO: 1416371-19-1
• Molecular Weight: 290.17
• Mol File: 1416371-19-1.mol

Chemical Properties

• CAS DataBase Reference: 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane(1416371-19-1)
• EPA Substance Registry System: 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane(1416371-19-1)

Safety Data

• Hazardous Substances Data: 1416371-19-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane is used as a reactant in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its ability to facilitate these bond formations makes it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane is used as a key intermediate in the production of various drugs. Its reactivity and structural properties allow for the creation of novel pharmaceutical compounds with potential therapeutic benefits.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane serves as an essential reactant in the synthesis of agrochemicals. Its role in creating new compounds contributes to the development of more effective and targeted pest control agents.
Used in Materials Science:
5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane also has potential applications in materials science. Its unique boron-containing structure may be utilized in the development of new materials with specific properties, such as improved thermal stability or enhanced electrical conductivity.
Used as a Reagent in Chemical Research:
In the field of chemical research, 5,5-dimethyl-2-(phenanthren-9-yl)-1,3,2-dioxaborinane is employed as a reagent to explore new chemical reactions and mechanisms. Its versatility and reactivity make it a valuable tool for advancing scientific understanding and discovering new chemical processes.

Upstream product

• 573-17-1 9-bromophenanthrene 
• 1589038-24-3 1-(phenanthren-9-yl)pyrrolidin-2-one 
• 201733-56-4 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane 
• 1228374-18-2 phenanthren-9-yl pivalate 
• 484-17-3 9-Phenanthrol 
• 1228374-20-6 4-(phenanthren-9-yl)morpholine 
• 68572-87-2 9-phenanthrenylboronic acid 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 

Relevant articles and documents

Direct Borylation of Tertiary Anilines via C-N Bond Activation

The first successful catalytic borylation of unactivated aromatic C-N bonds of tertiary anilines without the preactivation or any directing groups is demonstrated. The reactivity of both N,N-dialkylarylamines and N-arylpyrroles were investigated systematically, and the targeted products were furnished in moderate to good yields. The DFT calculation results indicated that the catalytic cycle is furnished via a five-membered cyclic transition-state due to the steric hindrance of the Ni/NHC catalytic system.

METHOD FOR PRODUCING ARYLBORONIC ACID ALKYLENE DIOL ESTER CRYSTALS

PROBLEM TO BE SOLVED: To provide an economical and industrially advantageous method for obtaining an arylboronic acid alkylene diol ester of high purity, especially one having a remarkably low halogen content. SOLUTION: Provided is a method for producing a C5-25 arylboronic acid alkylene diol ester crystals, comprising: step A of producing a C5-25 aryl boronic acid alkylene diol ester by reacting a C3-20 arylboronic acid and a C2-5 alkylene diol in organic solvent; and step B of precipitating the C5-25 arylboronic acid alkylene diol ester obtained in step A in the reaction solution of the above step. COPYRIGHT: (C)2015,JPOandINPIT

Rhodium-catalyzed borylation of aryl and alkenyl pivalates through the cleavage of carbonoxygen bonds

Rhodium-catalyzed borylation reactions of aryl and alkenyl pivalates, using a diboron reagent, via the cleavage of carbonoxygen bonds have been developed. The inert nature of the pivalate moiety enables relatively complex aryl boronates to be synthesized via the tandem cross-coupling of carbonhalogen and carbonoxygen bonds.

Nickel-catalyzed reductive and borylative cleavage of aromatic carbon-nitrogen bonds in N-aryl amides and carbamates

The nickel-catalyzed reaction of N-aryl amides with hydroborane or diboron reagents resulted in the formation of the corresponding reduction or borylation products, respectively. Mechanistic studies revealed that these reactions proceeded via the activation of the C(aryl)-N bonds of simple, electronically neutral substrates and did not require the presence of an ortho directing group.