1 acenaphthenol

Manufactured by Merck Group

1-acenaphthenol is a chemical compound used in various laboratory applications. It is a crystalline solid with a melting point of approximately 98-100°C. 1-acenaphthenol is commonly used as a chemical intermediate and in the synthesis of other organic compounds. However, a detailed and unbiased description of its core function without extrapolation on intended use cannot be provided concisely.

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Lab products found in correlation

R sulforaphane sfn, by LKT Laboratories (1 mentions) Menadione, by Merck Group (1 mentions) Androsterone, by Steraloids (1 mentions) Nicotinamide adenine dinucleotide nad, by Roche (1 mentions) Nicotinamide adenine dinucleotide phosphate nadp, by Roche (1 mentions) Rotenone, by Merck Group (1 mentions)

Close spelling variants of this product

Acenaphthenol

2 protocols using 1 acenaphthenol

Synthesis and Characterization of 3-NBA and 3-ABA

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3-NBA and 3-ABA were synthesized as described previously.^{28 (link),29 (link)} The purity and identity of these compounds were verified by UV spectroscopy, high-resolution mass spectrometry, and high-field 1H NMR spectroscopy. All other chemicals were of the highest grade commercially available, and all solvents were of HPLC grade. (S)-(+)-1,2,3,4-tetrahydro-1-naphthol (S-tetralol), flavin adenine dinucleotide (FAD), dithiothreitol (DTT), 1-acenaphthenol, dicoumarol (Dic), menadione, and D-glucose-6-phosphate (G6P) were purchased from Millipore-Sigma (St. Louis, MO). Glucose-6-phosphate dehydrogenase (G6PD) from Leuconostoc mesenteroides was purchased from Worthington Biochemical Corporation (Lakewood, NJ). 1-(2-Cyano-3,12,28-trioxooleana-1,9(11)-dien-28-yl)-1H-imidazole (CDDO-Im) was purchased from Tocris Bioscience (Bristol, U.K.) and R-sulforaphane (SFN) was purchased from LKT Laboratories (St. Paul, MN).

Murray J.R., de la Vega L., Hayes J.D., Duan L, & Penning T.M. (2019). Induction of the Antioxidant Response by the Transcription Factor NRF2 Increases Bioactivation of the Mutagenic Air Pollutant 3-Nitrobenzanthrone in Human Lung Cells. Chemical research in toxicology, 32(12), 2538-2551.

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Synthesis and Characterization of Nitro-Aromatic Compounds

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3-NBA, N-OH-3-ABA, and 3-ABA were synthesized as
described previously.^{31 (link),57 (link),58 (link)} The synthesis of 3-NOBA was performed from 3-ABA
following the experimental protocol reported by Fifer et al. for the synthesis
of similar nitroso-PAHs.^{59 (link)} The
purity and identity of these compounds were verified by UV spectroscopy, high
resolution mass spectrometry, and high-field ^{1 (link)} H NMR spectroscopy. All other chemicals were of the
highest grade available, and all solvents were of HPLC grade.
(S)-(+)-1,2,3,4-Tetrahydro-1-naphthol
(S-tetralol), flavin adenine dinucleotide (FAD), dithiothreitol
(DTT), 1-acenaphthenol, dicoumarol (Dic), allopurinol, rotenone, and
D-glucose-6-phosphate (G6P) were purchased from Millipore-Sigma (St. Louis, MO).
Nicotinamide adenine dinucleotide (NAD⁺) and nicotinamide adenine
dinucleotide phosphate (NADP⁺) were purchased from Roche Diagnostics
(Indianapolis, IN). Glucose-6-phosphate dehydrogenase (G6PD) was purchased from
Worthington Biochemical Corporation (Lakewood, NJ). Androsterone was purchased
from Steraloids (Wilton, NH); 2,6-dichloroindophenol (DCPIP) and salicylic acid
were purchased from Acros Organics (Geel, Belgium). Flufenamic acid (FA),
ursodeoxycholate, and indomethacin were purchased from ICN Biomedicals, Inc.
(Aurora, Ohio).

Murray J.R., Mesaros C.A., Arlt V.M., Seidel A., Blair I.A, & Penning T.M. (2018). Role of Human Aldo-Keto Reductases in the Metabolic Activation of the Carcinogenic Air Pollutant 3-Nitrobenzanthrone. Chemical research in toxicology, 31(11), 1277-1288.

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