2-Naphthaleneacetic acid, 5,6-dihydro-7-(1H-imidazol-1-yl)-

Base Information

Chemical Name:2-Naphthaleneacetic acid, 5,6-dihydro-7-(1H-imidazol-1-yl)-
CAS No.:89782-09-2
Molecular Formula:C₁₅H₁₄N₂O₂
Molecular Weight:254.288
Hs Code.:
DSSTox Substance ID:DTXSID00237899
Nikkaji Number:J419.960J
Wikidata:Q83120165

Synonyms:BRN 4320201;2-Naphthaleneacetic acid, 5,6-dihydro-7-(1H-imidazol-1-yl)-;7-(1H-Imidazol-1-yl)-5,6-dihydro-2-naphthaleneacetic acid;89782-09-2;SCHEMBL9812346;DTXSID00237899;LS-94301;5,6-Dihydro-7-(1H-imidazol-1-yl)naphthalene-2-acetic acid

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-Naphthaleneacetic acid, 5,6-dihydro-7-(1H-imidazol-1-yl)-

Chemical Property:

Vapor Pressure:6.31E-11mmHg at 25°C
Boiling Point:502.7°Cat760mmHg
Flash Point:257.8°C
Density:1.28g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:254.105527694
Heavy Atom Count:19
Complexity:380

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=CC2=C1C=CC(=C2)CC(=O)O)N3C=CN=C3

Technology Process of 2-Naphthaleneacetic acid, 5,6-dihydro-7-(1H-imidazol-1-yl)-

There total 7 articles about 2-Naphthaleneacetic acid, 5,6-dihydro-7-(1H-imidazol-1-yl)- 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:

: 89781-55-5
5,6-dihydro-7-(1H-imidazol-1-yl)-2-naphthalenecarboxylic acid

: 89782-09-2
5,6-dihydro-7-(1H-imidazol-1-yl)-2-naphthaleneacetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 72 percent / SOCl₂ / 24 h / Heating

2: 88.5 percent / LiAlH₄ / tetrahydrofuran / 24 h / Heating

3: SOCl₂, pyridine / CH₂Cl₂ / 3 h / Heating

4: H₂O; ethanol / 3 h / 100 °C

5: 23percent aq. HCl / 8 h / Heating

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1016/0223-5234(91)90103-T

Reference yield:

: 85929-03-9
2-(1-imidazolyl)-1,2,3,4-tetrahydro-7-carboxy-1-naphthalenol

: 89782-09-2
5,6-dihydro-7-(1H-imidazol-1-yl)-2-naphthaleneacetic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 71 percent / conc. H₂SO₄ / acetic acid / 4 h / 100 °C

2: 72 percent / SOCl₂ / 24 h / Heating

3: 88.5 percent / LiAlH₄ / tetrahydrofuran / 24 h / Heating

4: SOCl₂, pyridine / CH₂Cl₂ / 3 h / Heating

5: H₂O; ethanol / 3 h / 100 °C

6: 23percent aq. HCl / 8 h / Heating

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; In tetrahydrofuran; ethanol; dichloromethane; water; acetic acid;
DOI:10.1016/0223-5234(91)90103-T

Reference yield:

: 89781-89-5
5,6-dihydro-7-(1H-imidazol-1-yl)-2-naphthalenemethanol

: 89782-09-2
5,6-dihydro-7-(1H-imidazol-1-yl)-2-naphthaleneacetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂, pyridine / CH₂Cl₂ / 3 h / Heating

2: H₂O; ethanol / 3 h / 100 °C

3: 23percent aq. HCl / 8 h / Heating

With pyridine; hydrogenchloride; thionyl chloride; In ethanol; dichloromethane; water;
DOI:10.1016/0223-5234(91)90103-T