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31181-90-5

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31181-90-5 Usage

Description

5-Bromopyridine-2-carbaldehyde is an organic compound that serves as an important intermediate in the synthesis of various organic chemicals. It is characterized by its light yellow crystalline appearance and is known for its reactivity in chemical reactions, making it a valuable component in the development of new compounds and materials.

Uses

Used in Organic Chemical Synthesis:
5-Bromopyridine-2-carbaldehyde is used as an organic chemical synthesis intermediate for the production of a wide range of compounds. Its unique structure and reactivity allow it to be a key component in the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Bromopyridine-2-carbaldehyde is used as a building block for the development of new drugs. Its ability to participate in various chemical reactions enables the synthesis of diverse drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
5-Bromopyridine-2-carbaldehyde also finds application in the agrochemical industry, where it is utilized as a starting material for the synthesis of pesticides, herbicides, and other crop protection agents. Its versatility in chemical reactions allows for the development of innovative and effective products to protect crops from pests and diseases.
Used in Research and Development:
In the field of research and development, 5-Bromopyridine-2-carbaldehyde is employed as a valuable compound for exploring new chemical reactions and understanding the underlying mechanisms. Its unique properties make it an attractive candidate for studying various aspects of organic chemistry and contributing to the advancement of scientific knowledge.
Used in Material Science:
5-Bromopyridine-2-carbaldehyde can also be used in the field of material science, where it may contribute to the development of new materials with specific properties. Its reactivity and structural features can be exploited to create novel materials with applications in various industries, such as electronics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 31181-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,8 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31181-90:
(7*3)+(6*1)+(5*1)+(4*8)+(3*1)+(2*9)+(1*0)=85
85 % 10 = 5
So 31181-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrNO/c7-5-1-2-6(4-9)8-3-5/h1-4H

31181-90-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H50154)  5-Bromopyridine-2-carboxaldehyde, 99%   

  • 31181-90-5

  • 1g

  • 852.0CNY

  • Detail
  • Alfa Aesar

  • (H50154)  5-Bromopyridine-2-carboxaldehyde, 99%   

  • 31181-90-5

  • 5g

  • 4259.0CNY

  • Detail
  • Aldrich

  • (694177)  5-Bromo-2-pyridinecarboxaldehyde  95%

  • 31181-90-5

  • 694177-1G

  • 733.59CNY

  • Detail

31181-90-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromopyridine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Bromo-2-formylpyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31181-90-5 SDS

31181-90-5Relevant articles and documents

Simultaneous Generation of a [2 × 2] Grid-Like Complex and a Linear Double Helicate: a Three-Level Self-Sorting Process

Ayme, Jean-Fran?ois,Lehn, Jean-Marie,Bailly, Corinne,Karmazin, Lydia

, p. 5819 - 5824 (2020)

Two constitutional dynamic libraries (CDLs) - each containing two amines, two dialdehydes, and two metal salts - have been found to self-sort, generating two pairs of imine-based metallosupramolecular architectures (sharing no component) each with a [2 ×

Modeling the syn disposition of nitrogen donors in non-heme diiron enzymes. Synthesis, characterization, and hydrogen peroxide reactivity of diiron(III) complexes with the syn N-donor ligand H2BPG2DEV

Friedle, Simone,Kodanko, Jeremy J.,Morys, Anna J.,Hayashi, Takahiro,Moenne-Loccoz, Pierre,Lippard, Stephen J.

, p. 14508 - 14520 (2009)

In order to model the syn disposition of histidine residues in carboxylate-bridged non-heme diiron enzymes, we prepared a new dinucleating ligand, H2BPG2DEv, that provides this geometric feature. The ligand incorporates biologically

Enhancement of 4-electron O2 reduction by a Cu(II)-pyridylamine complex via protonation of a pendant pyridine in the second coordination sphere in water

Kotani, Hiroaki,Yagi, Tomomi,Ishizuka, Tomoya,Kojima, Takahiko

, p. 13385 - 13388 (2015)

We have synthesised a novel copper(II) complex with a pyridine pendant as a proton relay port for electrocatalytic 4e- reduction of O2 in water. The enhancement of the electrocatalytic O2 reduction via protonation of the pyridine pendant is demonstrated in comparison with a copper(II) complex without the pyridine pendant.

Synthesis of new Zn (II) complexes for photo decomposition of organic dye pollutants, industrial wastewater and photo-oxidation of methyl arenes under visible-light

Ahemed, Jakeer,Bhongiri, Yadagiri,Chetti, Prabhakar,Gade, Ramesh,Kore, Ranjith,Pasha, Jakeer,Pola, Someshwar,Rao D, Venkateshwar

, (2021/07/28)

Synthesis of new Schiff's base Zn-complexes for photo-oxidation of methyl arenes and xylenes are reported under visible light irradiation conditions. All the synthesized new ligands and Zn-complexes are thoroughly characterized with various spectral analyses and confirmed as 1:1 ratio of Zn and ligand with distorted octahedral structure. The bandgap energies of the ligands are higher than its Zn-complexes. These synthesized new Zn(II) complexes are used for the photo-fragmentation of organic dye pollutants, photodegradation of food industrial wastewater and oxidation of methyl arenes which are converted into its respective aldehydes with moderate yields under visible light irradiation. The photooxidation reaction dependency on the intensity of the visible light was also studied. With the increase in the dosage of photocatalyst, the methyl groups are oxidized to get aldehydes and mono acid products, which are also identified from LC-MS data. Finally, [Zn(PPMHT)Cl] is with better efficiency than [Zn(PTHMT)Cl] and [Zn(MIMHPT)Cl] for oxidation of methyl arenes is reported under visible-light-driven conditions.

A Simple, Mild and General Oxidation of Alcohols to Aldehydes or Ketones by SO2F2/K2CO3 Using DMSO as Solvent and Oxidant

Zha, Gao-Feng,Fang, Wan-Yin,Leng, Jing,Qin, Hua-Li

supporting information, p. 2262 - 2267 (2019/04/17)

A practical, general and mild oxidation of primary and secondary alcohols to carbonyl compounds proceeds in yields of up to 99% using SO2F2 as electrophile in DMSO as both the oxidant and the solvent at ambient temperature. No moisture- and oxygen-free conditions are required. Stoichiometric amount of inexpensive K2CO3, which generates easy to separate by-products, is used as the base. Thus, 5-gram scale runs proceeded in nearly quantitative yields by a simple filtration as the work-up. The use of a polar solvent such as DMSO, which usually promotes competing Pummerer rearrangement, is also noteworthy. This protocol is compatible with a variety of common N-, O-, and S-functional groups on (hetero)arene, alkene and alkyne substrates (68 examples). The protocol was applied (99% yield) to a formal synthesis of the important cholesterol-lowering drug Rosuvastatin. (Figure presented.).

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