215872-62-1

Basic information

• Product Name: 1H-Imidazole-5-methanol,1-ethyl-(9CI)
• Synonyms: 1H-Imidazole-5-methanol,1-ethyl-(9CI);(1-ethyl-1H-imidazol-5-yl)methanol(SALTDATA: FREE);1-Ethyl-1H-iMidazole-5-Methanol;1-Ethyl-1H-iMidazol-5-yl)Methanol
• CAS NO: 215872-62-1
• Molecular Formula: C6H10N2O
• Molecular Weight: 126.158
• Product Categories: AMINETERTIARY
• Mol File: 215872-62-1.mol

Chemical Properties

• Boiling Point: 321.9 °C at 760 mmHg
• Flash Point: 148.5 °C
• Appearance: /
• Density: 1.12 g/cm³
• Vapor Pressure: 0.000119mmHg at 25°C
• Refractive Index: 1.541
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.37±0.10(Predicted)
• CAS DataBase Reference: 1H-Imidazole-5-methanol,1-ethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-5-methanol,1-ethyl-(9CI)(215872-62-1)
• EPA Substance Registry System: 1H-Imidazole-5-methanol,1-ethyl-(9CI)(215872-62-1)

Safety Data

• Hazardous Substances Data: 215872-62-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1H-Imidazole-5-methanol,1-ethyl-(9CI) is used as a building block for the synthesis of various drugs due to its versatile chemical structure and reactivity. It contributes to the development of new therapeutic agents by providing a foundation for chemical modifications and enhancements.
Used in Organic Chemistry:
As a reagent, 1H-Imidazole-5-methanol,1-ethyl-(9CI) is utilized in various organic synthesis processes, facilitating the creation of complex organic molecules and compounds.
Used in Antifungal and Antibacterial Medications:
1H-Imidazole-5-methanol,1-ethyl-(9CI) is used as a precursor in the development of antifungal and antibacterial medications. Its potential applications in these areas stem from its chemical properties that can be harnessed to combat microbial infections.
Used in Medicinal Chemistry Research:
1H-Imidazole-5-methanol,1-ethyl-(9CI) is used in research for its potential antimicrobial and antiprotozoal properties. This makes it an important compound in the field of medicinal chemistry, where it can be studied and optimized for use in treating a range of diseases caused by microorganisms and parasites.

InChI:InChI=1/C6H10N2O/c1-2-8-5-7-3-6(8)4-9/h3,5,9H,2,4H2,1H3

Upstream product

• 71925-10-5 methyl 1-ethyl-1H-imidazole-5-carboxylate 
• 98412-27-2 1-ethyl-2-mercapto-5-hydroxymethyl-imidazole 

Downstream Products

• 790654-82-9 1-ethyl-5-chloromethylimidazole 

Relevant articles and documents

Efficient synthesis of 1-substituted-5-hydroxymethylimidazole derivatives: Clean oxidative cleavage of 2-mercapto group

1-Substituted-5-hydroxymethylimidazoles were prepared through green desulfurization of their 2-mercapto derivatives by the treatment of 30% hydrogen peroxide in the presence of a catalytic amount of transition metal catalysts.

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.

Process for preparing a 1-substituted 5-hydroxymethyl imidazole

A process for preparing a 1-substituted 5-hydroxymethylimidazole of the formula: , wherein R represents alkyl, hydroxyalkyl, allyl, or substituted or unsubstituted arylmethyl or diarylmethyl, comprising the step of reacting a 1-substituted 2-mercapto-5-hy

Substituted 1,2,4-triazolo[3,4-a]phthalazine derivatives as GABA alpha 5 ligands

Substituted 1,2,4-Triazolo[3,4-A]phthalazine derivatives are GABA Alpha 5 ligands and are represented by the formula