Some scientific research about 1-Phenylpiperidine-4-carbaldehyde

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Quality Control of: 1-Phenylpiperidine-4-carbaldehyde, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 111153-74-3

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent， Quality Control of: 1-Phenylpiperidine-4-carbaldehyde, Which mentioned a new discovery about 111153-74-3

The invention relates to the compounds of the formula STR1 wherein the C(=NH)–NHR group may be in tautomeric or isomeric form, and pharmaceutically acceptable salts thereof, in which: R is hydrogen or an acyl radical which is derived from an organic carbonic acid, an organic carboxylic acid, a sulfonic acid, or a carbamic acid; R1 is a substituent selected from an aliphatic hydrocarbon radical, an araliphatic hydrocarbon radical and a cycloaliphatic hydrocarbon radical; X1 and X3, independently of one another, are oxygen (–O–) or sulphur (–S–); and X2 is a divalent aliphatic hydrocarbon radical which may be interrupted by an aromatic radical; wherein the phenyl rings of formula I may be, independently of one another, further substituted by one or more substituents selected from halogen, trifluoromethyl, an aliphatic hydrocarbon radical, hydroxy, and hydroxy which is etherified by an aliphatic, araliphatic or cycloaliphatic alcohol or which is esterified by an aliphatic or araliphatic carboxylic acid; wherein aryl in the above definitions may be, independently of one another, further substituted by one or more substituents selected from halogen, trifluoromethyl, an aliphatic hydrocarbon radical, hydroxy, and hydroxy which is etherified by an aliphatic, araliphatic or cycloaliphatic alcohol or which is esterified by an aliphatic or araliphatic carboxylic acid; and wherein a cycloaliphatic hydrocarbon radical may be substituted by an aliphatic radical. The compounds are useful as selective LTB4 receptor antagonists in the treatment of conditions or syndromes in mammals which are responsive to LTB4 receptor antagonism.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Quality Control of: 1-Phenylpiperidine-4-carbaldehyde, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 111153-74-3

Reference：
Piperidine – Wikipedia,
Piperidine | C5H11704N – PubChem