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Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-4-cyanobenzyl bromide is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Bromo-4-cyanobenzyl bromide serves as a crucial building block for the creation of novel agrochemicals, such as pesticides and herbicides, that can improve crop protection and yield.
Used in Organic Chemistry Research:
2-Bromo-4-cyanobenzyl bromide is used as a versatile reagent in organic chemistry research for the formation of carbon-carbon, carbon-nitrogen, and carbon-oxygen bonds. Its ability to undergo nucleophilic aromatic substitution reactions makes it a valuable tool for the development of new chemical compounds and the exploration of novel reaction pathways.
Used in Material Science:
2-Bromo-4-cyanobenzyl bromide can be utilized in the development of new materials with specific properties, such as high thermal stability or unique electronic characteristics, by incorporating its structure into polymers or other composite materials.

InChI:InChI=1/C8H5Br2N/c9-4-7-2-1-6(5-11)3-8(7)10/h1-3H,4H2

Upstream product

• 7697-26-9 3-bromo-4-methylbenzoic acid 
• 42872-74-2 3-bromo-4-methyl-benzonitrile 

Downstream Products

• 89891-69-0 3-bromo-4-formyl benzonitrile 
• 90110-98-8 3-bromo-4-(hydroxymethyl)benzonitrile 
• 628686-21-5 3-Bromo-4-[(4-cyano-phenyl)-(3-methyl-3H-imidazol-4-yl)-methoxymethyl]-benzonitrile 
• 90004-92-5 3-Brom-terephthalaldehydamid 
• 91760-66-6 3-bromo-4-formyl-benzoic acid 
• 90221-60-6 2-Brom-4-hydroxymethyl-benzoesaeure 
• 90484-53-0 3-bromo-4-formyl-benzoic acid methyl ester 
• 1189765-90-9 3-Bromo-4-(bromomethyl)benzaldehyde 
• 1261679-15-5 C₉H₅BrN₂ 
• 1195621-94-3 1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborole-6-carbaldehyde 
• 947162-60-9 1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborole-6-carbonitrile 
• 1268336-25-9 4-cyano-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate 
• 201342-56-5 (2-bromo-4-cyanophenyl)methyl acetate 

Relevant academic research and scientific papers

Discovery of benzhydrol-oxaborole derivatives as Streptococcus pneumoniae leucyl-tRNA synthetase inhibitors

Pneumonia caused by bacterium S. pneumoniae is a severe acute respiratory infectious disease with high morbidity and mortality, especially for children and immunity-compromised patients. The emergence of multidrug-resistant S. pneumoniae also presents a c

A NEW TYPE OF BENZOXABOROLE-BASED ANTI-PNEUMOCOCCAL COMPOUNDS TARGETING LEUCYL-TRNA SYNTHETASE

Provided is benzoxaborole-based derivatives and their preparation and use. The structural general formula of the derivatives is (I). The derivatives are used for the preparation of a medicament for the prevention and treatment of Pneumonia. Compared with

Cross-coupling strategy for the synthesis of diazocines

Ethylene bridged azobenzenes are novel, promising molecular switches that are thermodynamically more stable in the (Z) than in the (E) configuration, contrary to the linear azobenzene. However, their previous synthetic routes were often not general, and yields were poorly reproducible, and sometimes very low. Here we present a new synthetic strategy that is both versatile and reliable. Starting from widely available 2-bromobenzyl bromides, the designated molecules can be obtained in three simple steps.

GLUCOSE SENSITIVE INSULIN DERIVATIVES

The present invention relates to novel insulin derivatives and their use in the treatment or prevention of medical conditions relating to diabetes. The insulin derivatives are glucose sensitive and display glucose-sensitive albumin binding. The invention

A general method for selective recognition of monosaccharides and oligosaccharides in water

Molecular recognition of carbohydrates plays vital roles in biology but has been difficult to achieve with synthetic receptors. Through covalent imprinting of carbohydrates in boroxole-functionalized cross-linked micelles, we prepared nanoparticle receptors for a wide variety of mono- and oligosaccharides. The boroxole functional monomer bound the sugar templates through cis-1,2-diol, cis-3,4-diol, and trans-4,6-diol. The protein-sized nanoparticles showed excellent selectivity for daldohexoses in water with submillimolar binding affinities and completely distinguished the three biologically important hexoses (glucose, mannose, and galactose). Glycosides with nonpolar aglycon showed stronger binding due to enhanced hydrophobic interactions. Oligosaccharides were distinguished on the basis of their monosaccharide building blocks, glycosidic linkages, chain length, as well as additional functional groups that could interact with the nanoparticles.

MICROBIOCIDAL BENZOXABOROLES

Compounds of formula (I) are as defined in the claims, and their use in compositions and methods for the control and/or prevention of microbial infection, particularly fungal infection, in plants and to processes for the preparation of these compounds.

Pesticidal compositions and processes related thereto

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

2-ARYL SELENAZOLE COMPOUND AND PHARMACEUTICAL COMPOSITION THEREOF

Disclosed are a 2-aryl selenazole compound and a pharmaceutical composition thereof, where the 2-aryl selenazole compound is a compound represented by formula (I) or a pharmaceutically acceptable salt thereof. The 2-aryl selenazole compound has the activi

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula ("Formula One"): and processes associated therewith.