856850-57-2 Usage
Description
6-Diethylamino-2-bromopyridine is a chemical compound with the molecular formula C9H14BrN2. It is a pyridine derivative featuring a bromine substituent and two ethylamino groups, primarily serving as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it is utilized in research and development applications.
Used in Pharmaceutical Industry:
6-Diethylamino-2-bromopyridine is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Diethylamino-2-bromopyridine is employed as a precursor in the production of agrochemicals, aiding in the creation of substances that protect crops and enhance agricultural productivity.
Used in Organic Compounds Synthesis:
6-Diethylamino-2-bromopyridine is utilized as a building block in the synthesis of a range of organic compounds, expanding the scope of chemical research and innovation.
Used in Research and Development:
6-DIETHYLAMINO-2-BROMOPYRIDINE is also used in research and development applications, where it can be explored for potential new uses, properties, and reactions, furthering scientific understanding and technological advancement.
It is important to handle and store 6-Diethylamino-2-bromopyridine with care, as it is a hazardous chemical that may pose risks to human health and the environment if not managed properly.
Check Digit Verification of cas no
The CAS Registry Mumber 856850-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,8,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 856850-57:
(8*8)+(7*5)+(6*6)+(5*8)+(4*5)+(3*0)+(2*5)+(1*7)=212
212 % 10 = 2
So 856850-57-2 is a valid CAS Registry Number.
856850-57-2Relevant articles and documents
Air-Stable Pd Catalytic Systems for Sequential One-Pot Synthesis of Challenging Unsymmetrical Aminoaromatics
Shaya, Janah,Deschamps, Marie-Angélique,Michel, Beno?t Y.,Burger, Alain
, p. 7566 - 7573 (2016/09/09)
The selective functionalization of dibromoaromatic scaffolds using air-stable palladium catalytic systems was carried out. This methodology involved rapid mono and diselective Buchwald-Hartwig aminations via microwave irradiation. The conditions were optimized to couple sequentially different moieties in one pot. Couplings with a wide scope of amines allowed accessing a new library of symmetrical and unsymmetrical derivatives (35 examples). Using this versatile method, a near-IR push-pull sensor was prepared installing the electron-donating and -withdrawing groups through a multicomponent reaction. These conditions revealed to be gram-scalable and adaptable to various groups; hence, promoting facile use in synthetic chemistry.
Regioselective intramolecular electrophilic substitution reactions involving π-deficient pyridine substrates: a new entry to pyridoquinazolines and benzo[h][1,6]naphthyridines
Agarwal, Piyush K.,Saifuddin, Mohammad,Kundu, Bijoy
experimental part, p. 862 - 870 (2010/03/25)
Regioselective intramolecular electrophilic substitution reactions have been described in π-deficient pyridine substrates tethered at C-2 to the aryl amine. The presence and nature of ring activating groups at C-6 led to the involvement of either N-1 or C-3 of the pyridine ring in the cyclization thereby leading to the regioselective synthesis of pyridoquinazolines and naphthyridines in excellent yields.
