1609374-04-0

Basic information

• Product Name: 2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine
• Synonyms: 2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine
• CAS NO: 1609374-04-0
• Molecular Weight: 309.173
• Mol File: 1609374-04-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 440.7±40.0 °C(Predicted)
• Density: 1.17±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine(1609374-04-0)
• EPA Substance Registry System: 2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine(1609374-04-0)

Safety Data

• Hazardous Substances Data: 1609374-04-0(Hazardous Substances Data)

Usage

General Description

2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine is a chemical compound that belongs to the benzofuro[2,3-b]pyridine family. It contains a 2-methyl-8 substituted with a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group. 2-methyl-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuro[2,3-b]pyridine has potential applications in the pharmaceutical industry as a building block for the synthesis of biologically active compounds. It can also be used in organic synthesis and medicinal chemistry for the development of new drugs.

Upstream product

• 1824-81-3 2-Amino-6-methylpyridine 
• 42753-71-9 5-bromo-6-methyl-pyridin-2-ylamine 
• 958357-86-3 2-amino-5-bromo-3-iodo-6-methylpyridine 
• 1609373-95-6 3-(2,3-dimethoxyphenyl)-6-methylpyridin-2-amine 
• 1609373-96-7 8-methoxy-2-methylbenzofuro[2,3-b]pyridine 
• 1609373-97-8 2-methylbenzofuro[2,3-b]pyridine-8-ol 
• 1609373-98-9 2-methylbenzofuran[2,3-b]pyridin-8-yl-trifluoromethanesulfonate 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 1609374-07-3 2-ethyl-8-(4-phenylpyridin-2-yl)benzofuro[2,3-b]pyridine 
• 1609374-08-4 2-isopropyl-8-(4-phenylpyridin-2-yl)benzofuro[2,3-b]pyridine 
• 1609368-36-6 C₄₇H₃₈IrN₄O 
• 1609368-37-7 C₄₉H₃₆⁽²⁾H₆IrN₄O 
• 1609368-54-8 C₄₅H₃₄IrN₄O 
• 1609368-55-9 C₄₇H₃₈IrN₄O 
• 1609374-03-9 8-(4-(3-isopropylphenyl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine 
• 1609368-35-5 C₄₈H₄₀IrN₄O 
• 1609374-13-1 2-methyl-8-(4-(p-tolyl)pyridin-2-yl)benzofuro[2,3-b]pyridine 
• 1609374-17-5 2-methyl-8-(5-phenylpyridin-2-yl)benzofuro[2,3-b]pyridine 
• 1609374-18-6 8-(4-(3,4-difluorophenyl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine 
• 1609368-45-7 C₄₅H₃₂F₂IrN₄O 
• 1609374-23-3 8-(4-(2-fluorophenyl)pyridin-2-yl)-2-methylbenzofuro[2,3-b]pyridine 
• 1609368-49-1 C₄₅H₃₃FIrN₄O 

Relevant articles and documents

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

Provided are organometallic compounds. Also provided are formulations comprising these organometallic compounds. Further provided are OLEDs and related consumer products that utilize these organometallic compounds.

Synthesis method of nitrogen-containing deuterated methyl compound

The invention discloses a synthesis method of a nitrogen-containing deuterated methyl compound. The method comprises the following steps: 2-amino-6-methylpyridine used as an initial raw material reacts with an aprotic solution of N-bromosuccinimide, separation is performed to obtain a compound 1, the compound 1 is subjected to an iodination reaction, palladium catalysis, cyclization, hydroxyl trifluoromethanesulfonic acid anhydridization and a deuteration reaction, and then extraction, organic phase mixing, saturated salt water washing, drying, spin-drying, column separation and other post-treatments to obtain the final product. The raw material has a low cost and is easy to obtain, so compared with other synthesis routes, the synthesis method of the nitrogen-containing deuterated methyl compound has the advantages of obvious reduction of the cost, good separation effect, few impurities, suitableness for large-scale production, and increase of the demethylation synthesis yield; the deuterated product can be effectively obtained through method, the deuteration rate can reach 97%, the production temperature is not higher than 100 DEG C to easily achieve safe production, and the practical value is high.