773134-84-2

Usage

Uses

Used in Pharmaceutical Industry:
Naphthalenecarboxylic acid, 1-bromo-, ethyl ester is used as a chemical intermediate for the production of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, Naphthalenecarboxylic acid, 1-bromo-, ethyl ester is employed as an intermediate in the synthesis of agrochemicals, which are essential for enhancing crop protection and productivity.
Used in Aromatic Chemicals Production:
Naphthalenecarboxylic acid, 1-bromo-, ethyl ester is used as a key intermediate in the production of aromatic chemicals, which are widely used in the fragrance, flavor, and chemical industries.
Used in Organic Synthesis:
Naphthalenecarboxylic acid, 1-bromo-, ethyl ester is used as a solvent in the synthesis of other organic compounds, facilitating various chemical reactions and contributing to the creation of new molecules.
Used in High-Performance Polymers Production:
As a chemical intermediate, Naphthalenecarboxylic acid, 1-bromo-, ethyl ester plays a role in the production of high-performance polymers, which are utilized in various industries due to their superior properties.
It is crucial to handle and use Naphthalenecarboxylic acid, 1-bromo-, ethyl ester with caution, as it can be toxic if ingested or inhaled and may cause irritation upon contact with the skin or eyes.

Upstream product

• 20717-79-7 1-bromo-2-naphthoic acid 
• 75-03-6 ethyl iodide 
• 127349-02-4 1-bromo-2-(dibromomethyl)naphthalene 
• 3378-82-3 1-bromo-2-naphthaldehyde 
• 2586-62-1 1-bromo-2-methylnaphtalene 
• 64-17-5 ethanol 

Downstream Products

• 1350966-06-1 C₃₅H₂₂ 
• 1350967-38-2 9-phenyl-7H-benzo[c]fluoren-7-one 

Relevant academic research and scientific papers

Synthesis of Axially Chiral 2,2′-Bisphosphobiarenes via a Nickel-Catalyzed Asymmetric Ullmann Coupling: General Access to Privileged Chiral Ligands without Optical Resolution

We report an asymmetric homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates resulting in highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates. These products are readily converted to enantioenriched b

INFLUENZA VIRUS REPLICATION INHIBITOR AND USE THEREOF

Disclosed are a compound as shown in formula (I) as an influenza virus replication inhibitor and a preparation method therefor, a pharmaceutical composition comprising the compound and the use of the compound and pharmaceutical composition thereof in the treatment of influenza.

New fluorescent blue oled host and dopant materials based on the spirobenzofluorene

New spiro[benzo[c]fluorene-7,9'-fluorene] (SBFF)-based blue host materials, 9-phenyl-SBFF (BH-4P) and 5,9-diphenyl-SBFF (BH-6DP), were successfully prepared by spiro-formation of 9-phenyl-7H-benzo[c]fluoren- 7-one with 2-bromobiphenyl via lithiation and reaction of 5,9-dibromo-SBFF with phenylboronic acid through the Suzuki reaction, respectively. Diphenyl-[4-(2-[1,1;4,1]terphenyl-4-yl-vinyl)-phenyl]-amine (BD-1) and N,N-diphenyl-N',N'-diphenyl-SBFF-5,9-diamine (BD-6DPA) were used as dopant materials. Blue OLEDs with the configuration ITO/N,N'-bis-[4-(di-m-tolylamino) phenyl]-N,N'-diphenylbiphenyl-4,4'-diamine (DNTPD)/ bis[N-(1-naphthyl)-N-phenyl] benzidine (NPB)/host:5% dopant/SFC-137/Al-LiF were prepared from the two host materials doped with BD-1 and BD-6DPA dopants and the devices composed of BH-4P and BH-6DP doped with BD-6DPA showed blue EL spectra at 458 and 463 nm at 7 V and luminance efficiencies of 4.58 and 4.88 cd/A, respectively.