7115-90-4

Usage

Uses

Used in Pharmaceutical Industry:
2-(bromoMethyl)benzoyl chloride is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing ones. Its unique structure allows for the creation of novel chemical entities with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(bromoMethyl)benzoyl chloride is utilized as a reagent in the production of agrochemicals, such as pesticides and herbicides. Its involvement in the synthesis process aids in the development of more effective and targeted agricultural chemicals to protect crops and enhance yield.
Used in Organic Synthesis:
2-(bromoMethyl)benzoyl chloride is employed as a versatile building block in organic synthesis, enabling the creation of a wide range of organic compounds with diverse applications. Its bromomethyl group facilitates various chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Fine Chemicals Production:
As a fine chemicals intermediate, 2-(bromoMethyl)benzoyl chloride plays a crucial role in the production of specialty chemicals with specific applications in industries such as fragrances, dyes, and coatings. Its unique properties allow for the development of high-quality and specialized products.
Safety Precautions:
Due to the high reactivity of 2-(bromoMethyl)benzoyl chloride, it is essential to handle 2-(broMoMethyl)benzoyl chloride with care and use it under proper safety precautions in a laboratory setting. This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and following established safety protocols to minimize risks associated with its use.

Upstream product

• 87-41-2 2-benzofuran-1(3H)-one 
• 7115-89-1 2-(bromomethyl)benzoic acid 

Downstream Products

• 7115-91-5 2-ethoxycarbonylbenzyl bromide 
• 77287-54-8 2--1,2-dihydroisoquinaldonitrile 
• 78482-05-0 2-tellurophthalide 
• 328937-14-0 C₅₆H₅₈O₁₂ 
• 328937-12-8 2-((2S,3R,4S,5R,6R)-3-Benzyloxy-6-benzyloxymethyl-5-hydroxy-2-methoxy-tetrahydro-pyran-4-yloxymethyl)-benzoic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-ethylsulfanyl-tetrahydro-pyran-3-yl ester 
• 749153-56-8 2-(Hydroxyaminomethyl)-benzoesaeure 
• 62758-46-7 2-(N-Carbethoxy-N-hydroxyaminomethyl)-benzoesaeure 
• 62758-48-9 C₁₇H₂₇N₃O₄ 
• 62758-47-8 N-Hydroxy-N-<(2-benzylaminocarbonyl)phenylmethyl>-carbaminsaeureethylester 
• 54266-99-8 o-propoxycarbonylbenzyltributylphosphonium bromide 
• 872041-15-1 (2-Bromomethylphenyl)-(2,5-dimethoxyphenyl)methanone 
• 1235579-64-2 2-[(6-benzyl-5,8-dioxo-5,8-dihydropyrido-[2,3-d]pyridazin-7(6H)-yl)carbonyl]benzyltriphenylphosphonium bromide 
• 1235579-63-1 2-[(7-benzyl-5,8-dioxo-7,8-dihydropyrido-[2,3-d]pyridazin-6(5H)-yl)carbonyl]benzyltriphenylphosphonium bromide 
• 1235579-65-3 7-benzyl-6-{2-[(triphenylphosphoranilidene)methyl]benzoyl}-6,7-dihydropyrido-[2,3-d]pyridazine-5,8-dione 

Relevant academic research and scientific papers

Visible-Light-Mediated Late-Stage Sulfonylation of Anilines with Sulfonamides

A visible-light-mediated late-stage sulfonylation of anilines with sulfonamides under simple reaction conditions is presented. Various primary or secondary sulfonamides including several pharmaceuticals were incorporated successfully via N–S bond activati

Performance comparison of two cascade reaction models in fluorescence off-on detection of hydrogen sulfide

Comparative studies on the performances of two cascade reaction based fluorescent H2S probes are reported. These probes were also designed to address the solubility issues of existing probes. The Reso-N3 probe favors the H2S mediated azide-to-amine reduction followed by a cyclization to release the resorufin fluorophore. Reso-Br undergoes a bromide-to-thiol nucleophilic substitution followed by a similar cyclization releasing the same fluorophore. Reso-N3 exhibited lower background fluorescence and better H2S sensing behavior in water compared to Reso-Br. Reso-Br underwent hydrolysis in aqueous buffer conditions (pH = 7.4) while, Reso-N3 was quite stable. Reso-N3 displayed high selectivity and sensitivity towards H2S. Live cell imaging of the species by the probe was also established. This journal is

TETRAAZA-CYCLOPENTA[A]INDENYL AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS

The present invention provides compounds of Formula (I) as M1 receptor positive allosteric modulators for the treatment of diseases mediated by the muscarinic M1 mediator.

Synthesis of pyridazinedione derivatives starting from anhydrides of 2,3-pyridine-and 2,3-quinolinedicarboxylic acids

A method was developed of preparation of heterocyclic compounds with pyridopyridazinoiso-quinalinedione and isoquinopyridazinoquinalinedione structures formed regioselectively by intramolecular cyclization of phosphorus ylides containing pyridopyridazinedione and pyridazinoquinolinedione fragments. Pleiades Publishing, Ltd., 2010.

N-benzyl substituted pyridyl porphyrin compounds and methods of use thereof

The present invention relates to N-Benzyl-Substituted Pyridyl Porphyrin Compounds, compositions comprising an effective amount of an N-Benzyl-Substituted Pyridyl Porphyrin Compound and methods for treating or preventing injury due to exposure to a reactiv

Topical formulations for treating allergic diseases

Methods for topically treating allergic diseases of the eye, ear or nose using tricyclic compounds are disclosed.