7115-90-4

Basic information

• Product Name: 2-(broMoMethyl)benzoyl chloride
• Synonyms: 2-(broMoMethyl)benzoyl chloride
• CAS NO: 7115-90-4
• Molecular Formula: C₈H₆BrClO
• Molecular Weight: 233.48964
• Mol File: 7115-90-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 294.7±23.0 °C(Predicted)
• Appearance: /
• Density: 1.606±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-(broMoMethyl)benzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(broMoMethyl)benzoyl chloride(7115-90-4)
• EPA Substance Registry System: 2-(broMoMethyl)benzoyl chloride(7115-90-4)

Safety Data

• Hazardous Substances Data: 7115-90-4(Hazardous Substances Data)

Usage

General Description

2-(bromoMethyl)benzoyl chloride is a chemical compound with the formula C8H6BrClO. It is a benzoyl chloride derivative that contains a bromomethyl group attached to the benzene ring. 2-(broMoMethyl)benzoyl chloride is commonly used as a reagent in chemical reactions, particularly in the synthesis of various organic compounds. It is a versatile intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. 2-(bromoMethyl)benzoyl chloride is also used in the preparation of benzoyl derivatives, which are important building blocks in organic synthesis. Due to its high reactivity, it should be handled with care and used under proper safety precautions in a laboratory setting.

Upstream product

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

Downstream Products

• 62758-35-4 3-(3,4,5-trimethoxy-benzoyl)-3,4-dihydro-benzo[d][1,2]oxazin-1-one 
• 62758-37-6 3-(4-chloro-benzoyl)-3,4-dihydro-benzo[d][1,2]oxazin-1-one 
• 62758-53-6 3-benzoyl-3,4-dihydro-benzo[d][1,2]oxazin-1-one 
• 62758-36-5 3-(4-methyl-benzoyl)-3,4-dihydro-benzo[d][1,2]oxazin-1-one 

Relevant articles and documents

Synthesis of isoindolo[2,1-b]isoquinoline-5,7-dione via the wittig intramolecular cyclization

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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

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.