1159803-56-1

Basic information

• Product Name: 2-(3-Methyoxyphenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
• Synonyms: 2-(3-Methyoxyphenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
• CAS NO: 1159803-56-1
• Molecular Formula: C₁₇H₁₅BN₂O
• Molecular Weight: 274.1248
• Mol File: 1159803-56-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 467.5±47.0 °C(Predicted)
• Appearance: /
• Density: 1.22±0.1 g/cm3(Predicted)
• PKA: -2.80±0.20(Predicted)
• CAS DataBase Reference: 2-(3-Methyoxyphenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-Methyoxyphenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(1159803-56-1)
• EPA Substance Registry System: 2-(3-Methyoxyphenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(1159803-56-1)

Safety Data

• Hazardous Substances Data: 1159803-56-1(Hazardous Substances Data)

Usage

Molecular structure

A unique structure containing a naphthalene ring fused with a boron-containing diazaborinine ring.

Compound classification

Boron-containing heterocyclic compound.

Potential applications

Organic synthesis, materials science, pharmaceutical research and development (further studies needed).

Unique properties

Structural and electronic properties that make it a subject of interest for various research and industrial applications.

Upstream product

• 1214264-88-6 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine 
• 536-90-3 m-Anisidine 
• 2845-89-8 1-chloro-3-methoxy-benzene 
• 2398-37-0 3-methoxyphenyl bromide 
• 100-66-3 methoxybenzene 
• 5656-71-3 2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine 

Relevant articles and documents

Direct transformation from arylamines to aryl naphthalene-1,8-diamino boronamides: A metal-free sandmeyer-type process

A direct metal-free transformation from arylamines to aryl naphthalene-1,8-diamino boronamides, a type of masked boronic acid, has been developed based on Sandmeyer-type reactions. A nonsymmetrical diboron reagent, B(pin)-B(dan), was utilized as the boryl

Synthesis of masked haloareneboronic acids via iridium-catalyzed aromatic C-H borylation with 1,8-naphthalenediaminatoborane (danBH)

"Masked" areneboronic acids have been prepared by Ir-catalyzed C-H borylation of arenes. A [Ir(OMe)(cod)]2 complex with a DPPE ligand showed the highest catalytic activity in the C-H borylation of benzene at 80 °C. The reaction system can be ap