123876-53-9

Usage

Uses

Used in Pharmaceutical Synthesis:
Benzoyl chloride, 4-(3-bromopropyl)is used as a reagent in the synthesis of pharmaceuticals. Its unique structure allows for the formation of various drug molecules with specific therapeutic properties.
Used in Agrochemical Production:
Benzoyl chloride, 4-(3-bromopropyl)is also utilized in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Plasticizer Manufacturing:
Benzoyl chloride, 4-(3-bromopropyl)is employed in the manufacturing process of plasticizers, which are additives used to increase the flexibility and workability of plastics.
Used in Industrial Chemical Production:
Benzoyl chloride, 4-(3-bromopropyl)finds application in the production of various industrial chemicals, where its reactivity and unique structure contribute to the synthesis of specialized chemical products.

Upstream product

• 79-37-8 oxalyl dichloride 
• 637-59-2 1-Bromo-3-phenylpropane 
• 113100-86-0 4-(3-bromo-propyl)-benzoic acid methyl ester 
• 41996-96-7 1-(4-acetylphenyl)-3-bromopropane 
• 6309-79-1 4-(3-Bromo-propyl)-benzoic acid 

Downstream Products

• 401928-16-3 3-[4-(3-(dibutylamino)propyl)benzoyl]-2-butyl-1-benzofuran-5-carboxylic acid 
• 113100-86-0 4-(3-bromo-propyl)-benzoic acid methyl ester 

Relevant academic research and scientific papers

8-Phenyl-Substituted Dipyrromethene·Bf2 Complexes as Highly Efficient and Photostable Laser Dyes

We report on the synthesis and the photophysical and lasing properties of two new dipyrromethene·BF2 dyes, analogues of the commercial dye PM567, dissolved in liquid solutions or in polymeric matrices of poly(methyl methacrylate) and as solid c

Synthesis method of methyl 4-(3-bromopropyl)benzoate

The invention provides a synthetic method of methyl 4-(3-bromopropyl)benzoate, and relates to the field of medicinal chemistry. The invention provides a new scheme for synthesizing methyl 4-(3-bromopropyl)benzoate from 1-bromo-3-phenylpropane through a two-step one-pot method, and provides a new synthesis route for preparation and synthesis of methyl 4-(3-bromopropyl)benzoate. Moreover, accordingto the synthesis scheme, common raw materials are adopted as reactants, the reaction conditions are proper, the final product is synthesized with the cost remarkably reduced compared with the prior art, the preparation process is simple, the cost is low, large-scale production can be achieved, and a synthesis thought is provided for synthesis of the derivative of the compound.

A nitric oxide donor nature of the benzofuran compounds (by machine translation)

The invention discloses a benzofuran compound with nitrous oxide donor property. The benzofuran compound is a compound shown by a general formula (I) or a pharmaceutically acceptable salt thereof, wherein in the formula, R1 or R2 represents independent hy

PHENYL HYDROXAMIC ACIDS INCLUDING A HETERO-CONTAINING SUBSTITUENT

Phenyl hydroxamic acids are disclosed having the general formula or a pharmaceutically acceptable salt thereof, wherein X is NR, oxygen, sulfur, or a single bond, and Y is NR, oxygen, sulfur, or a single bond, where R can be hydrogen or lower alkyl, g can be 1 or 2, and with the proviso that at least one of X and Y is other than a single bond; Z is aryl, aralkyl or cycloalkyl; R1 is hydrogen, substituted or unsubstituted lower alkyl, cycloalkyl, lower alkenyl or aryl; R2 is hydrogen, lower alkyl, aroyl or acyl; m is 0 to 4 carbon atoms; and, n is 0 to 4 carbon atoms further providing that if one of X or Y is oxygen, the other of X or Y must be oxygen and further that when X and Y are oxygen Z cannot be aralalkyl. These new compounds have been found to be inhibitors or arachidonic acid 5-lipoxygenase and are therefore useful as antiallergy agents and antipsoriatics.