153836-44-3

Basic information

• Product Name: 1-(Azetidin-3-yl)-1H-iMidazole hydrochloride
• Synonyms: 1-(Azetidin-3-yl)-1H-iMidazole hydrochloride;1-(Azetidin-3-yl)-1H-imidazole 2HCl
• CAS NO: 153836-44-3
• Molecular Formula: C6H10ClN3
• Molecular Weight: 159.6167
• Mol File: 153836-44-3.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 1-(Azetidin-3-yl)-1H-iMidazole hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(Azetidin-3-yl)-1H-iMidazole hydrochloride(153836-44-3)
• EPA Substance Registry System: 1-(Azetidin-3-yl)-1H-iMidazole hydrochloride(153836-44-3)

Safety Data

• Hazardous Substances Data: 153836-44-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Applications:
1-(Azetidin-3-yl)-1H-imidazole hydrochloride is used as a potential pharmaceutical compound for its unique chemical properties. Although specific uses are not well documented, its categorization within the azetidines and imidazoles families suggests potential applications in drug development, given the prevalence of these structures in various bioactive molecules.

Relevant articles and documents

NOVEL PYRIDONE CARBOXYLIC ACID DERIVATIVE OR SALT THEREOF

It is intended to provide a novel compound having high antitumor activity and low toxicity to normal cells. The present invention provides a pyridone carboxylic acid derivative represented by the following formula (1) or a salt thereof wherein R1 represents a hydrogen atom, a halogen atom or the like; R2 represents a hydrogen atom, a halogen atom or the like; R3 to R6 each represent a hydrogen atom or the like; R7 represents a hydrogen atom or the like; R8 represents a hydrogen atom, a halogen atom, the following formula (a) (wherein Ra1 and Ra2 each represent a hydrogen atom, a hydroxy group, an optionally substituted lower alkyl group or the like) or the like, or R7 and R8 together represent —N—OR10 (wherein R10 represents a hydrogen atom, an optionally substituted lower alkyl group, or an aralkyl group), or R7 and R8 form an optionally substituted 4- to 6-membered saturated hetero ring together with the adjacent carbon atom, or the like; R9 represents a hydrogen atom or the like; X represents a nitrogen atom or the like; and Y represents a nitrogen atom or the like.

Antimicrobial carbapenem derivatives, their preparation and their therapeutic use

Compounds of formula (I): (in which R1 is hydrogen or methyl, R2 is hydrogen, optionally substituted aliphatic hydrocarbon or acylimidoyl, R3 is hydrogen or an ester group, and Q is an optionally quaternized nitrogen-containing group) are useful antibiotics which are resistant to dehydropeptidase I, and are thus useful for the treatment of many microbial infections.