1159803-51-6

Basic information

• Product Name: 2-(3-Methylphenyl)-2,3-dihydro-1H-naphtho-[1,8-de][1,3,2]diazaborinine
• Synonyms: 2-(3-Methylphenyl)-2,3-dihydro-1H-naphtho-[1,8-de][1,3,2]diazaborinine
• CAS NO: 1159803-51-6
• Molecular Formula: C₁₇H₁₅BN₂
• Molecular Weight: 258.1254
• Mol File: 1159803-51-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(3-Methylphenyl)-2,3-dihydro-1H-naphtho-[1,8-de][1,3,2]diazaborinine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-Methylphenyl)-2,3-dihydro-1H-naphtho-[1,8-de][1,3,2]diazaborinine(1159803-51-6)
• EPA Substance Registry System: 2-(3-Methylphenyl)-2,3-dihydro-1H-naphtho-[1,8-de][1,3,2]diazaborinine(1159803-51-6)

Safety Data

• Hazardous Substances Data: 1159803-51-6(Hazardous Substances Data)

Usage

Molecular structure

A complex structure containing a naphthalene ring fused to a diazaborinine ring, and a 3-methylphenyl group attached to the naphthalene ring.

Building block

Can be used for the synthesis of various boron-containing compounds.

Potential applications

Has potential applications in the fields of materials science, organic chemistry, and pharmaceutical research.

Unique structural features

Makes it of interest to researchers for its potential as a ligand in coordination chemistry and as a precursor for the synthesis of novel and complex organic molecules.

Upstream product

• 17933-03-8 m-tolylboronic acid 
• 479-27-6 naphthalene-1,8-diamine 
• 591-17-3 meta-bromotoluene 
• 5656-71-3 2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine 
• 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 
• 108-44-1 1-amino-3-methylbenzene 
• 108-88-3 toluene 

Downstream Products

• 7383-90-6 3,4'-dimethylbiphenyl 

Relevant articles and documents

Catalyst-free and eco-friendly synthesis of masked haloarylboronic acids R (alkyl or aryl)-B(dan) on water

An environment-friendly methodology for the synthesis of R (alkyl or aryl)-B(dan) on water is described. 1,8-diamino naphthalene(danH2) was reacted with different types of organoboronic acids to furnish the products in moderate to excellent yields. A multi-gram scale reaction is also performed to ensure the scalability of the reaction.

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