1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol, (-)-

Base Information

• Chemical Name: 1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol, (-)-
• CAS No.: 27656-21-9
• Molecular Formula: C11H10Cl2N2O
• Molecular Weight: 257.119
• European Community (EC) Number: 608-122-1
• UNII: C0YOQ871FJ
• DSSTox Substance ID: DTXSID60182033
• Nikkaji Number: J2.946.710B
• Wikidata: Q27275028
• Mol file: 27656-21-9.mol

Synonyms:27656-21-9;(R)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol;UNII-C0YOQ871FJ;C0YOQ871FJ;1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol, (-)-;(-)-alpha-(2,4-Dichlorophenyl)-1H-imidazole-1-ethanol;Imidazole-1-ethanol, alpha-(2,4-dichlorophenyl)-, (-)-;1H-Imidazole-1-ethanol, alpha-(2,4-dichlorophenyl)-, (R)-;1H-Imidazole-1-ethanol, alpha-(2,4-dichlorophenyl)-, (alphaR)-;SCHEMBL4664843;DTXSID60182033;Q27275028;(-)-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol;(1R)-1-(2,4-Dichlorophenyl)-2-(1H-imidazole-1-yl)ethanol;(-)-.ALPHA.-(2,4-DICHLOROPHENYL)-1H-IMIDAZOLE-1-ETHANOL;IMIDAZOLE-1-ETHANOL, .ALPHA.-(2,4-DICHLOROPHENYL)-, (-)-;1H-IMIDAZOLE-1-ETHANOL, .ALPHA.-(2,4-DICHLOROPHENYL)-, (R)-;1H-IMIDAZOLE-1-ETHANOL, .ALPHA.-(2,4-DICHLOROPHENYL)-, (.ALPHA.R)-

Chemical Property of 1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol, (-)-

Chemical Property:

• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 256.0170183
• Heavy Atom Count: 16
• Complexity: 230

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1Cl)Cl)C(CN2C=CN=C2)O
• Isomeric SMILES: C1=CC(=C(C=C1Cl)Cl)[C@H](CN2C=CN=C2)O

Technology Process of 1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol, (-)-

There total 11 articles about 1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol, (-)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.0%

1H-imidazole (288-32-4) + (R)-2-chloro-1-(2',4'-dichlorophenyl)-1-ethanol (114446-57-0) → (R)-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol (27656-21-9)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 100 ℃; for 3h;

DOI:10.1021/jo102459w

Reference yield: 77.0%

1H-imidazole (288-32-4) + (R)-2-(2,4-dichlorophenyl)oxirane (62566-67-0) → (R)-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol (27656-21-9)

Guidance literature:

In 1,4-dioxane; at 100 ℃; for 16h; regioselective reaction;

DOI:10.1021/jo102459w

Reference yield: 37.0%

1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-ol (24155-42-8) → (R)-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanol (27656-21-9)

Guidance literature:

1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-ol; With D-tartaric acid; In methanol; acetone; at 20 ℃; for 0.5h;

With sodium hydroxide; water; In dichloromethane;

upstream raw materials:

1H-imidazole

(R)-2-(2,4-dichlorophenyl)oxirane

1-(2,4-dichlorophenyl)-2-(imidazol-1-yl)ethanone

2,2',4'-trichloroacetophenone

Downstream raw materials:

C₂₆H₃₈Cl₂N₂O₃

(R)-1-[2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole

(-)-Miconazole