25023-22-7

Basic information

• Product Name: IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER
• Synonyms: IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER;Methyl 2-(Imidazol-1-yl)acetate;Methyl 2-(1-IMidazolyl)acetate;1H-IMidazole-1-acetic acid, Methyl ester
• CAS NO: 25023-22-7
• Molecular Formula: C₆H₈N₂O₂
• Molecular Weight: 140.14
• Mol File: 25023-22-7.mol
• Article Data: 15

Chemical Properties

• Melting Point: 55 °C
• Boiling Point: 282.5°C at 760 mmHg
• Flash Point: 124.6°C
• Appearance: /
• Density: 1.17g/cm³
• Vapor Pressure: 0.00335mmHg at 25°C
• Refractive Index: 1.529
• Storage Temp.: 2-8°C
• PKA: 6.21±0.10(Predicted)
• CAS DataBase Reference: IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER(25023-22-7)
• EPA Substance Registry System: IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER(25023-22-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 25023-22-7(Hazardous Substances Data)

Usage

General Description

IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER is a chemical compound with the molecular formula C6H8N2O2. It is a methyl ester derivative of imidazole-1-ylacetic acid, an imidazole compound that contains both an imidazole ring and a carboxylic acid group. This chemical is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds. It is known for its potential biological and pharmacological activities, making it a valuable building block in drug development and medicinal chemistry. Due to its versatile properties, IMIDAZOL-1-YL-ACETIC ACID METHYL ESTER is a widely utilized chemical in various research and industrial applications.

InChI:InChI=1/C6H8N2O2/c1-10-6(9)4-8-3-2-7-5-8/h2-3,5H,4H2,1H3

Upstream product

• 288-32-4 1H-imidazole 
• 6773-29-1 dimethyl diazomalonate 
• 96-34-4 methyl chloroacetate 
• 96-32-2 bromoacetic acid methyl ester 
• 18156-74-6 1-(Trimethylsilyl)imidazole 

Downstream Products

• 22884-10-2 imidazol-1-ylacetic acid 
• 1225209-30-2 C₂₇H₂₇N₃O₅ 

Relevant articles and documents

Hydroxyethyl and ester co-functionalized imidazolium iodide for highly efficient solid-state dye-sensitized solar cells

Hydroxyethyl and ester co-functionalized imidazolium iodide has been designed and synthesized as an efficient solid state electrolyte for dye-sensitized solar cells. Single crystal X-ray analyses confirm the presence of ordered three dimensional ionic channels for iodide, which exhibits high conductivity when mixed with iodine and LiI and achieves a power conversion efficiency of 7.45%.

POSS with eight imidazolium iodide arms for efficient solid-state dye-sensitized solar cells

Polyhedral oligomeric silsesquioxane functionalized with eight imidazolium iodide arms has been designed and synthesized for use as solid-state electrolytes in solid-state dye-sensitized solar cells, which exhibits a power conversion efficiency of 7.11% under one sun illumination and good long-term stability under one sun soaking.

Development of imidazole alkanoic acids as mGAT3 selective GABA uptake inhibitors

A new series of potential GABA uptake inhibitors starting from of 1H-imidazol-4-ylacetic acid with the carboxylic acid side chain originating from different positions and varying in length have been synthesized and tested for the inhibitory potency at the