144385-79-5

Basic information

• Product Name: 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr)
• Synonyms: 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr);1-(3-broMopropyl)-1H-iMidazole HBr salt;1-(3-Bromopropyl)-1H-imidazole hydrobromide;1-(3-bromopropyl)-1H-imidazole
• CAS NO: 144385-79-5
• Molecular Formula: C₆H₉BrN₂
• Molecular Weight: 269.965
• Mol File: 144385-79-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr)(144385-79-5)
• EPA Substance Registry System: 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr)(144385-79-5)

Safety Data

• Hazardous Substances Data: 144385-79-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr) is used as an intermediate in the synthesis of various pharmaceuticals. The presence of the bromine atom allows it to participate in nucleophilic substitution reactions, making it a valuable building block for the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr) is utilized as a key intermediate for the synthesis of various agrochemicals. Its reactivity and structural features contribute to the creation of effective compounds for agricultural applications.
Used in Organic Chemistry:
1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr) is used as a reagent in organic chemistry due to its ability to undergo nucleophilic substitution reactions. This property makes it a versatile compound for the synthesis of a wide range of organic molecules.
Used in Medicinal Chemistry:
The imidazole ring structure of 1-(3-bromopropyl)-1H-imidazole(SALTDATA: HBr) gives it potential biological activity, making it a valuable compound for medicinal chemistry research. It can be used to develop new drugs with specific therapeutic targets.
Used in Salt Form Applications:
The hydrobromide (HBr) salt form of 1-(3-bromopropyl)-1H-imidazole enhances its solubility and stability, making it suitable for various applications where improved solubility is required, such as in drug formulations or chemical reactions.

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