38993-84-9

Basic information

• Product Name: (1-METHYL-1H-IMIDAZOL-5-YL)METHANOL
• Synonyms: RARECHEM AL BD 0940;(3-METHYL-3H-IMIDAZOL-4-YL)-METHANOL;5-HYDROXYMETHYL-1-METHYL-1H-IMIDAZOLE;(1-METHYL-1H-IMIDAZOL-5-YL)METHANOL;1-METHYL-5-(HYDROXYMETHYL)IMIDAZOLE;5-(HydroxyMethyl)-1-MethyliMidazole;(3-methylimidazol-4-yl)methanol;1H-Imidazole-5-methanol,1-methyl-
• CAS NO: 38993-84-9
• Molecular Formula: C₅H₈N₂O
• Molecular Weight: 112.13
• Product Categories: blocks;Imidazoles;Imidazol&Benzimidazole
• Mol File: 38993-84-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 113 °C
• Boiling Point: 324.872 °C at 760 mmHg
• Flash Point: 150.278 °C
• Appearance: /
• Density: 1.167 g/cm³
• Vapor Pressure: 9.76E-05mmHg at 25°C
• Refractive Index: 1.552
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: DMSO (Sparingly), Methanol (Slightly)
• PKA: 14.35±0.10(Predicted)
• CAS DataBase Reference: (1-METHYL-1H-IMIDAZOL-5-YL)METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (1-METHYL-1H-IMIDAZOL-5-YL)METHANOL(38993-84-9)
• EPA Substance Registry System: (1-METHYL-1H-IMIDAZOL-5-YL)METHANOL(38993-84-9)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39-37/39-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 38993-84-9(Hazardous Substances Data)

Usage

General Description

"(1-Methyl-1H-imidazol-5-yl)methanol", also known by its CAS number 82294-70-6, is a chemical compound with the formula C5H8N2O. It belongs to the class of organic compounds known as imidazole alkaloids, which are alkaloids with a structure based on the imidazole ring, a five-membered ring with two non-adjacent nitrogen atoms. Specific details about this chemical, such as its appearance, density, boiling and melting points, differ depending on the source. Information about its toxicological and safety properties is not widely available, which suggests that it is not widely used or studied. Being an organic compound, it likely undergoes typical organic reactions, but detailed information about its reactivity and uses are not widely available. Identified as a potentially novel chemical entity, it could potentially be used in the development of new pharmaceuticals, although more research is needed to determine its properties and potential applications.

InChI:InChI=1/C5H8N2O/c1-7-4-6-2-5(7)3-8/h2,4,8H,3H2,1H3

Upstream product

• 96-26-4 dihydroxyacetone 
• 5041-09-8 isobutylamine hydrochloride 
• 22680-44-0 (2-chlorophenyl)methanamine monohydrochloride 
• 42365-42-4 3-chloro-benzylamine; hydrochloride 
• 42365-50-4 3-methyl-benzylamine; hydrochloride 
• 26177-45-7 4-methylbenzylamine hydrochloride 
• 18600-40-3 (2-methoxyethyl)amine hydrochloride 
• 50877-01-5 cyclohexanmethylamine hydrochloride 
• 41806-40-0 1-methyl-1H-imidazole-5-carboxylic acid 
• 822-55-9 (1H-imidazol-4-yl)methanol 

Downstream Products

• 89180-90-5 5-(chloromethyl)-1-methyl-1H-imidazole 
• 41065-01-4 1-Methyl-5-cyanomethyl-imidazol 
• 141524-74-5 4-bromo-1-methyl-1H-imidazole-5-carbaldehyde 
• 1608158-79-7 4-chloro-1-[(3-methylimidazol-4-yl)methyl]-3,5-diphenyl-pyrazolo[3,4-c]pyridazine 
• 1569071-04-0 C₁₇H₂₅FN₂O₂Si 
• 499770-71-7 5-(bromomethyl)-1-methyl-1H-imidazole 
• 1196072-08-8 3-(4-(N,N-bis-(2-chloroethyl)amino)phenoxysulfonyl-(N-methylimidazol-5-yl-methyl))methyl-2-nitrothiophene 
• 158629-34-6 [3-Methyl-2-(4-nitro-benzoyl)-3H-imidazol-4-yl]-acetonitrile 
• 158629-24-4 (5-Hydroxymethyl-1-methyl-1H-imidazol-2-yl)-(4-nitro-phenyl)-methanone 

Relevant articles and documents

Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof

The present invention relates to a novel imidazole derivative represented by formula (1) which shows an inhibitory activity against farnesyl transferase or pharmaceutically acceptable salts or isomers thereof, in which A, n1and Y are defined in the specification; to a process for preparation of the compound of formula (1); to intermediates which are used in the preparation of the compound of formula (1); and to a pharmaceutical composition comprising the compound of formula (1) as an active ingredient.