33214-18-5

Basic information

• Product Name: 1-propyl-2-MethyliMidazole
• Synonyms: 1-propyl-2-MethyliMidazole;1H-Imidazole, 2-methyl-1-propyl-
• CAS NO: 33214-18-5
• Molecular Formula: C₇H₁₂N₂
• Molecular Weight: 124.18358
• Mol File: 33214-18-5.mol

Chemical Properties

• Appearance: solid or liquid
• CAS DataBase Reference: 1-propyl-2-MethyliMidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-propyl-2-MethyliMidazole(33214-18-5)
• EPA Substance Registry System: 1-propyl-2-MethyliMidazole(33214-18-5)

Safety Data

• Hazardous Substances Data: 33214-18-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-Propyl-2-methylimidazole is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to facilitate the production of these compounds.
Used as a Corrosion Inhibitor:
1-Propyl-2-methylimidazole is used as a corrosion inhibitor in various industrial applications to protect materials from degradation and extend their lifespan.
Used as a Catalyst in Chemical Reactions:
1-Propyl-2-methylimidazole is used as a catalyst in chemical reactions to speed up the process and improve the efficiency of the reactions.
Used as a Solvent in Industrial Processes:
1-Propyl-2-methylimidazole is used as a solvent in various industrial processes due to its ability to dissolve a wide range of substances.
Used in Antimicrobial and Antifungal Applications:
1-Propyl-2-methylimidazole is used for its antimicrobial and antifungal properties, making it useful in applications such as disinfectants and preservatives.
Used in Food Industry:
1-Propyl-2-methylimidazole is considered relatively safe for human consumption and is not known to be carcinogenic or mutagenic, making it suitable for use in the food industry as a preservative or flavoring agent.

InChI:InChI=1S/C7H12N2/c1-3-5-9-6-4-8-7(9)2/h4,6H,3,5H2,1-2H3

Upstream product

• 693-98-1 2-methylimidazole 
• 107-08-4 1-iodo-propane 
• 106-94-5 propyl bromide 

Relevant articles and documents

METHOD FOR PRODUCING IONIC LIQUID AND METHOD FOR PRODUCING INTERMEDIATE BODY FOR PRODUCTION OF IONIC LIQUID

PROBLEM TO BE SOLVED: To provide a method for producing an ionic liquid for synthesizing a desired ionic liquid with high purity, and to provide a method for producing an intermediate body for synthesizing the ionic liquid. SOLUTION: A method for producing an ionic liquid which produces a desired ionic liquid Q+Z- formed from cation Q+ and anion Z- includes: a step of purifying a high-melting point intermediate body Q+Y- that is formed from the cation Q+ and the anion Z- and has such a melting point as to be recrystallized, by recrystallization; and a step of obtaining the ionic liquid Q+Z- directly or indirectly from the purified high-melting point intermediate body Q+Y-. A method for producing a strongly acidic intermediate body and a super-hydrophilic intermediate body includes: a step of obtaining a strongly acidic intermediate body or a super-hydrophilic intermediate body from the purified high-melting point intermediate body Q+Y- by a double decomposition precipitation method or obtaining the strongly acidic intermediate body from the purified high-melting point intermediate body Q+Y- by a double decomposition precipitation method, or a step of obtaining the super-hydrophilic intermediate body from the strongly acidic intermediate body by a neutralization method. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2018,JPOandINPIT

BENZAZEPINE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE

The present invention provides a novel benzazepine derivative represented by formula : wherein, R1 is a 5- or 6-membered aromatic ring, R2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula -W1-X2-W2- (W1 and W2 are independently S(O)m1 (m1 is 0, 1 or 2), etc., and X2 is an optionally substituted alkylene groupetc. ), a preparation method and use thereof.