164330-69-2

Basic information

• Product Name: ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate
• Synonyms: ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate;1H-IMidazole-4-carboxylic acid, 1-(2-aMino-5-Methylphenyl)-5-Methyl-, ethyl ester
• CAS NO: 164330-69-2
• Molecular Formula: C14H17N3O2
• Molecular Weight: 259.307
• Mol File: 164330-69-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 442.1°C at 760 mmHg
• Flash Point: 221.2°C
• Appearance: /
• Density: 1.2g/cm³
• Vapor Pressure: 5.16E-08mmHg at 25°C
• Refractive Index: 1.592
• PKA: 3.11±0.10(Predicted)
• CAS DataBase Reference: ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate(164330-69-2)
• EPA Substance Registry System: ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate(164330-69-2)

Safety Data

• Hazardous Substances Data: 164330-69-2(Hazardous Substances Data)

Usage

Description

Ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate is a complex chemical compound that features an imidazole ring and an ethyl ester group. Derived from imidazole, this compound incorporates an amino group and a methyl group, which contribute to its biological activity. Its unique structural features suggest potential pharmaceutical applications, enabling it to influence a range of biological processes.

Uses

Used in Pharmaceutical Applications:
Ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate serves as a biologically active compound for the development of pharmaceuticals, leveraging its structural attributes to modulate various biological processes. Its potential use in medicinal chemistry is significant, given its capacity to interact with biological targets and systems.
Used in Research Applications:
In the field of scientific research, ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate is utilized as a research chemical. It aids in the investigation of imidazole-based compounds and their effects on biological systems, contributing to the advancement of knowledge in medicinal chemistry and related disciplines.
Used in Industrial Applications:
Ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate may also find use in industrial applications, where its unique chemical properties can be harnessed for specific processes or the synthesis of other compounds. Its role in industry can be diverse, depending on the requirements of various chemical processes or the development of new materials.
It is crucial to handle ethyl 1-(2-amino-5-methylphenyl)-5-methyl-1H-imidazole-4-carboxylate with care and adhere to safety guidelines to ensure the safety of individuals and the environment.

InChI:InChI=1/C14H17N3O2/c1-4-19-14(18)13-10(3)17(8-16-13)12-7-9(2)5-6-11(12)15/h5-8H,4,15H2,1-3H3