210832-86-3

Usage

Chemical Properties

Yellow Solid

Uses

A highly flourescent compound

InChI:InChI=1/C14H14BrNO/c1-16(2)13-6-5-10-7-12(14(17)9-15)4-3-11(10)8-13/h3-8H,9H2,1-2H3

Upstream product

• 68520-00-3 1-(6-(dimethylamino)naphthalen-2-yl)ethan-1-one 
• 3900-45-6 6-methoxy-2-acetylnaphthalene 
• 210832-83-0 6,6'-dibromoacetyl-2-(dimethylamino)naphthalene 

Downstream Products

• 1552301-13-9 C₂₀H₁₉N₃O₄ 
• 1552301-15-1 2-(α-(3,4-diaminophenoxy)acetyl)-6-(dimethylamino)naphthalene 

Relevant academic research and scientific papers

Enantioselective synthesis and application of the highly fluorescent and environment-sensitive amino acid 6-(2-dimethylaminonaphthoyl) alanine (DANA).

6-(2-Dimethylaminonaphthoyl) alanine (DANA) was prepared via an enantioselective synthesis and incorporated into the S-peptide of RNase S establishing the large changes in fluorescence that can occur upon peptide-protein interaction.

Highly selective two-photon fluorescent probe for imaging of nitric oxide in living cells

A new two-photon fluorescent probe, ADNO, for nitric oxide (NO) based on intramolecular photoinduced electron transfer (PET) mechanism displays a rapid response to NO with a remarkable fluorescent enhancement in PBS buffer. The excellent chemoselectivity

A facile protocol for the convenient preparation of amino-substituted α-bromo- and α,α-dibromo arylmethylketones

Amino-substituted arylmethylketones are selectively brominated in sulfuric acid to afford the corresponding dibromomethylarylketones that are then debrominated with diethylphosphite to give the desired bromomethylarylketones in excellent yield.