870774-29-1

Basic information

• Product Name: 3-(naphthalene-2-yl)phenylboronic acid
• Synonyms: 3-(naphthalene-2-yl)phenylboronic acid;[3-(2-Naphthalenyl)phenyl]boronic acid;(3-(Naphthalen-2-yl)phenyl)boronic acid;B-[3-(2-naphthalenyl)phenyl]Boronic acid;3-(2-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride);(3-(Naphthalen-2-yl)
• CAS NO: 870774-29-1
• Molecular Formula: C₁₆H₁₃BO₂
• Molecular Weight: 248.08422
• Mol File: 870774-29-1.mol

Chemical Properties

• Boiling Point: 486.0±48.0 °C(Predicted)
• Appearance: /
• Density: 1.23±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.27±0.19(Predicted)
• CAS DataBase Reference: 3-(naphthalene-2-yl)phenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(naphthalene-2-yl)phenylboronic acid(870774-29-1)
• EPA Substance Registry System: 3-(naphthalene-2-yl)phenylboronic acid(870774-29-1)

Safety Data

• Hazardous Substances Data: 870774-29-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3-(naphthalene-2-yl)phenylboronic acid is used as a reagent in the Suzuki coupling reaction, a widely employed method for the formation of carbon-carbon bonds. This reaction is crucial for the synthesis of various organic compounds, including pharmaceuticals and organic materials.
Used in the Development of Organic Light-Emitting Diodes (OLEDs):
3-(naphthalene-2-yl)phenylboronic acid is utilized in the development of OLEDs due to its ability to form stable complexes with various substrates. Its incorporation in OLED materials can enhance the performance and efficiency of these devices, making it an essential component in the field of optoelectronics.
Used in Pharmaceutical Development:
3-(naphthalene-2-yl)phenylboronic acid is used in the development of pharmaceuticals, where its ability to form stable complexes with various substrates can contribute to the design and synthesis of new drug molecules. Its unique structure and reactivity make it a valuable tool in medicinal chemistry for creating novel therapeutic agents.

Upstream product

• 667940-23-0 2-(3-bromophenyl)naphthalene 
• 5419-55-6 Triisopropyl borate 
• 32316-92-0 naphthalene-2-boronic acid 

Downstream Products

• 944801-33-6 9-bromo-10-(3-(naphthalen-2-yl)phenyl)anthracene 

Relevant articles and documents

Scyllo-inositol as a convenient protecting group for aryl boronic acids in Suzuki-Miyaura cross-coupling reactions

Herein, we report air-and water-stable borate complexes between scyllo-inositol and aryl boronic acids. The complexes were less reactive than free aryl boronic acids under Suzuki-Miyaura cross-coupling reaction conditions; thus, the borate complexes were used as protected boronic acids. Although protecting groups for organoboronic acids are useful in coupling reactions, especially those used to produce π-conjugated molecules, only a few reports describing the use of protecting groups for boronic acids have been published. The proposed unique structural borate complex provides a novel protective method for aryl boronic acids.

PHENANTHRENE DERIVATIVE, AND MATERIAL FOR ORGANIC EL ELEMENT

A phenanthrene derivative is represented by a formula (1) below. In the formula (1), Ar1 and Ar2 each represent an aromatic hydrocarbon ring group having 6 to 18 carbon atoms for forming the ring. The aromatic hydrocarbon ring group contains none of anthracene skeleton, pyrene skeleton, aceanthrylene skeleton and naphthacene skeleton. R1 represents a substituent, the number of which may be 0, 1 or more. R1 may be bonded in any position of the phenanthrene skeleton. n and m each represent an integer of 1 to 3. k represents an integer of 0 to 8.

NAPHTHALENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE DEVICE, AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME

A naphthalene derivative represented by the following formula (1) is provided. In the formula, Ar1 to Ar4 each represent an aromatic hydrocarbon cyclic group having 6 to 18 carbon atoms forming a ring. The aromatic hydrocarbon cyclic group has none of anthracene skeleton, pyrene skeleton, aceanthrylene skeleton and naphthacene skeleton. n, m and 1 each represent an integer in a range of 1 to 5. p represents an integer in a range of o to 5. When n, m, 1 and p each are 2 or more, a plurality of Ar1 to Ar4 may be mutually the same or different.

NEW ANTHRACENE DERIVATIVES, PREPARATION METHOD THEREOF AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

The present invention provides a novel anthracene derivative, a method for preparing the same, and an organic electronic device using the same. The anthracene derivative according to the invention can function alone as a light emitting host, in particular, as a blue host in an organic electronic device. Further, the anthracene derivative according to the invention can also function as a hole injecting or hole transporting material, an electron injecting or electron transporting material, or a light emitting material in an organic electronic device including a light emitting device. Therefore, the organic electronic device according to the present invention shows excellent characteristics in efficiency, drive voltage and stability.