1-(1,2,3,4-Tetrahydro-7-methoxy-2-naphthalenyl)-1H-imidazole

Base Information

• Chemical Name: 1-(1,2,3,4-Tetrahydro-7-methoxy-2-naphthalenyl)-1H-imidazole
• CAS No.: 89781-82-8
• Molecular Formula: C₁₄H₁₆N₂O
• Molecular Weight: 228.294
• DSSTox Substance ID: DTXSID701008971
• Nikkaji Number: J759.054G

Synonyms:BRN 4752638;1-(1,2,3,4-Tetrahydro-7-methoxy-2-naphthalenyl)-1H-imidazole;1H-Imidazole, 1-(1,2,3,4-tetrahydro-7-methoxy-2-naphthalenyl)-;89781-82-8;SCHEMBL10895495;MQSABNQTUJJOKD-UHFFFAOYSA-N;DTXSID701008971;LS-78902;1,2,3,4-tetrahydro-2-(1-imidazolyl)-7-methoxy-naphthalene;1-(7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)-1H-imidazole;2-(1H-Imidazol-1-yl)-1,2,3,4-tetrahydro-7-methoxynaphthalene

Chemical Property of 1-(1,2,3,4-Tetrahydro-7-methoxy-2-naphthalenyl)-1H-imidazole

Chemical Property:

• Vapor Pressure: 1.65E-07mmHg at 25°C
• Boiling Point: 439.4°Cat760mmHg
• Flash Point: 219.5°C
• Density: 1.17g/cm³
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 228.126263138
• Heavy Atom Count: 17
• Complexity: 259

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC2=C(CCC(C2)N3C=CN=C3)C=C1

Technology Process of 1-(1,2,3,4-Tetrahydro-7-methoxy-2-naphthalenyl)-1H-imidazole

There total 6 articles about 1-(1,2,3,4-Tetrahydro-7-methoxy-2-naphthalenyl)-1H-imidazole 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: 85.0%

1,2-dihydro-3-(1-imidazolyl)-6-methoxynaphthalene (89781-56-6) → 1,2,3,4-tetrahydro-2-(1-imidazolyl)-7-methoxy-naphthalene (89781-82-8)

Guidance literature:

With hydrogenchloride; hydrogen; acetic acid; palladium on activated charcoal; In ethanol; for 12h; under 2585.7 Torr; Ambient temperature;

DOI:10.1016/0223-5234(91)90103-T

Reference yield: 53.0%

2-(1-imidazolyl)-3,4-dihydro-7-methoxy-1(2H)-naphthalenone (85928-58-1) → 1,2,3,4-tetrahydro-2-(1-imidazolyl)-7-methoxy-naphthalene (89781-82-8)

Guidance literature:

With perchloric acid; hydrogen; palladium on activated charcoal; In acetic acid; at 85 ℃; under 3750.3 Torr;

DOI:10.1002/ardp.19963290506

Reference yield:

1H-imidazole (288-32-4) + 3-bromo-6-methoxy-2,3-dihydro-4H-1-benzopyran-4-one (66125-08-4) → 3-(1H-imidazol-1-yl)-6-methoxy-2,3-dihydro-4H-1-benzopyran-4-one (80929-63-1) + 1,2,3,4-tetrahydro-2-(1-imidazolyl)-7-methoxy-naphthalene (89781-82-8)

Guidance literature:

With hydrogenchloride; In N,N-dimethyl-formamide;

upstream raw materials:

1,2-dihydro-3-(1-imidazolyl)-6-methoxynaphthalene

2-(1-imidazolyl)-3,4-dihydro-7-methoxy-1(2H)-naphthalenone

2-bromo-7-methoxy-3,4-dihydro-1(2H)-naphthalenone

2-(1-imidazolyl)-1,2,3,4-tetrahydro-7-methoxy-1-naphthalenol

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