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Usage

Uses

Used in Organic Synthesis:
2-(benzyloxy)-5-bromobenzonitrile is employed as a building block in organic synthesis, contributing to the formation of complex organic molecules. Its reactivity in coupling reactions makes it a valuable component in the synthesis of various compounds.
Used in Pharmaceutical Production:
2-(benzyloxy)-5-bromobenzonitrile is used as a reagent in the production of pharmaceuticals. Its presence in the synthesis process aids in the creation of new drug molecules, potentially leading to the development of novel treatments and therapies.
Used in Agrochemical Production:
2-(benzyloxy)-5-bromobenzonitrile is also utilized in the production of agrochemicals. Its role in the synthesis of these compounds can contribute to the development of new pesticides, herbicides, or other agricultural products, enhancing crop protection and yield.

Relevant academic research and scientific papers

2-PHENYLTHIOPHENE DERIVATIVE

The present invention relates to a 2-phenylthiophene derivative or a salt thereof, wherein the thiophene ring is substituted with a carboxyl group or the like and the benzene ring has an electron-withdrawing group such as a cyano group and an electron-donating group such as a substituted alkoxy group at the same time. Since the compound of the invention has good xanthine oxidase-inhibitory action and uric acid-lowering action and does not have a structure derived from nucleic acid, the compound has advantages of high safety and excellent effects as compared with conventional compounds and is useful as a therapeutic or preventive agent for hyperuricemia, gout, inflammatory bowel diseases, diabetic kidney diseases, diabetic retinopathy, or the like.

2-PHENYLPYRIDINE DERIVATIVE

A 2-phenylpyridine derivative represented by the following general formula (I) or a salt thereof. The compounds have satisfactory xanthine oxidase inhibitory activity and uric acid-lowering activity and are useful as a therapeutic or preventive agent for hyperuricemia, gout, inflammatory intestinal diseases, diabetic nephropathy, diabetic retinopathy, etc. [The symbols in the formula have the following meanings: R1: H, etc.; R2: -CO2H, etc.; R3 and R4: H, etc.; R5: -CN, etc.; R6: H, etc.; X: -O-, -N(R8)-, or -S-; (provided that the groups represented by R5 and -X-R7 are bonded in a meta position or the para position to the pyridyl group) R8: H, etc.; R7: C1-8 linear or branched alkyl, etc.; Y: a bond, etc.; and R9, R10, and R11: H, etc. (provided that when X is -N(R8)-, then R8 may be bonded to R7 to form a nitrogenous saturated heterocycle in cooperation with the adjacent nitrogen atom).]