1H-Imidazole, 2,5-dihydro-1-hydroxy-5,5-dimethyl-4-phenyl-, 3-oxide

Base Information

• Chemical Name: 1H-Imidazole, 2,5-dihydro-1-hydroxy-5,5-dimethyl-4-phenyl-, 3-oxide
• CAS No.: 59570-09-1
• Molecular Formula: C11H14N2O2
• Molecular Weight: 206.24100
• DSSTox Substance ID: DTXSID50355299
• Wikidata: Q82134097
• ChEMBL ID: CHEMBL1311037

Synonyms:59570-09-1;SMR000103178;1H-Imidazole, 2,5-dihydro-1-hydroxy-5,5-dimethyl-4-phenyl-, 3-oxide;MLS000106209;CHEMBL1311037;DTXSID50355299;HMS1580H21;HMS2440L16;STK834662;AKOS000534431;AB00081406-01;5,5-dimethyl-4-phenyl-2,5-dihydro-1H-imidazol-1-ol 3-oxide

Chemical Property of 1H-Imidazole, 2,5-dihydro-1-hydroxy-5,5-dimethyl-4-phenyl-, 3-oxide

Chemical Property:

• PSA: 52.22000
• LogP: 1.32360
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 206.105527694
• Heavy Atom Count: 15
• Complexity: 280

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C(=[N+](CN1O)[O-])C2=CC=CC=C2)C

Technology Process of 1H-Imidazole, 2,5-dihydro-1-hydroxy-5,5-dimethyl-4-phenyl-, 3-oxide

There total 1 articles about 1H-Imidazole, 2,5-dihydro-1-hydroxy-5,5-dimethyl-4-phenyl-, 3-oxide 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:

→ 1-hydroxy-5,5-dimethyl-4-phenyl-3-imidazoline 3-oxide (59570-09-1)

Guidance literature:

N-<1-Hydroxyimino-2-methyl-1-phenylpropyl-(2)>-hydroxylamin, Formadeldehyd;

Reference yield: 80.0%

ethanol (64-17-5) + 1-hydroxy-5,5-dimethyl-4-phenyl-3-imidazoline 3-oxide (59570-09-1) → C15H21N2O4 (104406-67-9) + 2,2-Diethoxy-5,5-dimethyl-3-oxy-4-phenyl-2,5-dihydro-imidazol-1-ol (124761-90-6) + 2-ethoxy-5,5-dimethyl-3-oxy-4-phenyl-2,5-dihydro-imidazol-1-ol (59570-10-4)

Guidance literature:

With lead dioxide; for 20h;

DOI:10.1007/BF00978444

Reference yield: 50.0%

1-hydroxy-5,5-dimethyl-4-phenyl-3-imidazoline 3-oxide (59570-09-1) → 4,4-dimethyl-5-phenyl-4H-imidazole 1,3-dioxide (104406-69-1)

Guidance literature:

With 4-phenyl-2,2,5,5-tetramethyl-3-imidazolin-1-yloxy-3-oxide; In chloroform; for 2h; Heating;

DOI:10.1007/BF00486679

Downstream raw materials:

C₁₇H₂₅N₂O₄

5,5-dimethyl-2,2-dimethoxy-4-phenyl-3-imidazoline 3-oxide-1-oxyl

5,5-dimethyl-2,4-dimethoxy-4-phenyl-2-imidazoline 1-oxyl

C₁₅H₂₁N₂O₄

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