90-15-3

1-Naphthol Chemical Structure
90-15-3

Chemical Structure

1-Naphthol

Synonym(s): Furro ER; NSC 9586; Nako TRB

  • CAS. Nr.: 90-15-3
  • Formula:C10H8O
  • Molecular Weight:144.17

IUPAC Name: naphthalen-1-ol

InChIKey: KJCVRFUGPWSIIH-UHFFFAOYSA-N

SMILES: OC1=C2C=CC=CC2=CC=C1

Biological Activity: 1-naphthol (Furro ER) is an excited state proton transfer (ESPT) fluorescent molecular probe. 1-naphthol can sense the hydrophobic domains in micellar aggregation and accurately sense the sol-gel transition. 1-naphthol can be used to study the thermally induced microenvironmental changes and hydration levels of Pluronic F127 (PF127) in different microenvironments in aqueous media[1].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-Y1309
1-Naphthol 99.90% 1-naphthol (Furro ER) is an excited state proton transfer (ESPT) fluorescent molecular probe. 1-naphthol can sense the hydrophobic domains in micellar aggregation and accurately sense the sol-gel transition. 1-naphthol can be used to study the thermally induced microenvironmental changes and hydration levels of Pluronic F127 (PF127) in different microenvironments in aqueous media.
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HY-Y1309R
1-Naphthol (Standard) ≥98% 1-Naphthol (Standard) is the analytical standard of 1-Naphthol. This product is intended for research and analytical applications. 1-naphthol is an excited state proton transfer (ESPT) fluorescent molecular probe.
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HY-Y1309S1
1-Naphthol-d7 99.44% 1-Naphthol-d7 (Furro ER-d7) is the deuterium labeled Naphthol (HY-Y1309). 1-Naphthol (Furro ER) is an excited state proton transfer (ESPT) fluorescent molecular probe. 1-naphthol can sense the hydrophobic domains in micellar aggregation and accurately sense the sol-gel transition. 1-naphthol can be used to study the thermally induced microenvironmental changes and hydration levels of Pluronic F127 (PF127) in different microenvironments in aqueous media.
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HY-128105
1,2-Dihydroxynaphthalene 98.88% 1,2-Dihydroxynaphthalene (1,2-Naphthalenediol) is a metabolic intermediate of Naphthalene and a precursor for the formation of 1,2-Naphthoquinone, and is also the most sensitive biomarker of Naphthalene exposure in humans. 1,2-Dihydroxynaphthalene inhibits the AMPK/SIRT3 pathway and activates acetylated p53 and NF-κB by inducing oxidative stress, leading to G2/M cell cycle arrest, senescence, and apoptosis, while also damaging DNA through the formation of depurination adducts, thereby causing mutations. 1,2-Dihydroxynaphthalene can be used in research on cancer and cataracts.
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HY-32126
1-Fluoronaphthalene 99.56% 1-Fluoronaphthalene is an organofluorine compound derived from naphthalene derivatives and fluorinated aromatics. 1-Fluoronaphthalene can be used to synthesize LY248686, a potent inhibitor of serotonin and noradrenaline uptake.
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HY-34235
2-Methyl-1-naphthol 2-Methyl-1-naphthol is a key precursor in the synthesis of Vitamin K3. 2-Methyl-1-naphthol is can be used for the research of Vitamin K Deficiency.
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HY-W007967
4-Chloro-1-naphthol 99.74% 4-Chloronaphthalen-1-ol is a substrate of horseradish peroxidase. 4-Chloronaphthalen-1-ol can be used to visualize protein bands in western blotting and immunohistochemical staining.
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HY-W131305
Naphthohydroquinone Naphthohydroquinone is a compound featuring a naphthalene ring structure with two hydroxyl groups. Naphthohydroquinone exhibits significant cytotoxicity and antitumor activity in some of its derivatives.
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HY-Y0110
2-Naphthol 99.89% 2-Naphthol is a metabolite of naphthalene, catalyzed by cytochrome P450 (CYP) isozymes (CYP 1A1, CYP 1A2, CYP 2A1, CYP 2E1 and CYP 2F2).
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HY-Y0825R
1,5-Dihydroxynaphthalene (Standard) ≥98% 1,5-Dihydroxynaphthalene (Standard) is the analytical standard of 1,5-Dihydroxynaphthalene. This product is intended for research and analytical applications.
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HY-Y1119R
1-Bromonaphthalene (Standard) ≥98% 1-Bromonaphthalene (Standard) is the analytical standard of 1-Bromonaphthalene. This product is intended for research and analytical applications. 1-Bromonaphthalene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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References