92-44-4
92-44-4
Chemical Structure
2,3-Dihydroxynaphthalene
Synonym(s): 2,3-Naphthalenediol
- CAS No.: 92-44-4
- Formula:C10H8O2
- Molecular Weight:160.17
IUPAC Name: naphthalene-2,3-diol
InChIKey: JRNGUTKWMSBIBF-UHFFFAOYSA-N
SMILES: OC1=CC2=CC=CC=C2C=C1O
Biological Activity: Naphthalene-2,3-diol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2,3-Dihydroxynaphthalene | 98.62% | Naphthalene-2,3-diol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Jineol | 99.68% | Jineol is a cytotoxic alkaloid from the centipede Scolopendra subspinipes. Jineol exhibits modest cytotoxic activity in vitro against the growth of human tumor cell lines. | ||||||||||||||||||||
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1,2-Dihydroxynaphthalene | 98.88% | 1,2-Dihydroxynaphthalene 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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2,3-Diaminonaphthalene | 98.12% | 2,3-Diaminonaphthalene is a fluorescent reagent used to detect selenium and nitric oxide (NO). 2,3-Diaminonaphthalene binds to selenium to form pyrazolene selenol, with excitation/emission maxima at 365 nm and 525 nm, respectively. 2,3-Diaminonaphthalene binds to NO2− to form the fluorescent product, 1-(H)-napthotriazole, with excitation/emission maxima at 360 nm and 440 nm, respectively. | ||||||||||||||||||||
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Naphthoresorcinol | 99.49% | Naphthoresorcinol (1,3-Dihydroxynaphthalene) is a fluorescent dye (λex=330 nm, λem=380 nm) that can react with the NPPD (a tracer) and concentrated HCl and develop a red color. Naphthoresorcinol could be used as a background electrolyte (BGE) to determine the carbohydrates. | ||||||||||||||||||||
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6-Bromo-2-naphthol | 99.75% | 6-Bromo-2-naphthol is an RTP (real-time polymerase chain reaction) probe that forms a 1:1 or 2:1 complex with β-cyclodextrin (β-CD). 6-Bromo-2-naphthol is capable of real-time monitoring of PCR reactions and quantification of specific nucleic acid sequences. RTP probes are a class of small DNA or RNA sequences labeled with fluorescent dyes and quencher molecules, which can be widely used in gene expression analysis, SNP genotyping, and pathogen detection. 6-Bromo-2-naphthol embeds into the cyclodextrin cavity through hydrophobic interactions, inhibits the oxygen quenching effect, and emits a phosphorescent signal at room temperature. 6-Bromo-2-naphthol can also be used as an intermediate for the synthesis of antibacterial azo dyes, and its derivatives show antibacterial activity against Staphylococcus aureus, Escherichia coli and other bacteria. | ||||||||||||||||||||
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2,7-Dihydroxynaphthalene | 99.27% | 2,7-Dihydroxynaphthalene (2,7-DHN) is a substrate of a new group of aromatic prenyltransferases in fungi and can be catalyzed to undergo a regiospecific prenylation reaction. 2,7-Dihydroxynaphthalene can undergo reactions such as oxidation and substitution. | ||||||||||||||||||||
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Menadiol | 97.0% | Menadiol (Dihydrovitamin K3) is a menadione analog that acts as an electron donor. Menadiol transfers electrons to the heme bL of E. coli nitrate reductase A and, via heme bH, to the catalytic NarGH dimer. Menadiol drives ATP-dependent NAD⁺ reduction (reverse electron transport) in submitochondrial particles. Menadiol selectively inhibits the growth of lymphoid tumor cells. Menadiol enhances the growth-inhibitory effects of Mechlorethamine, Vincristine (HY-N0488A), and Dexamethasone (HY-14648) on tumor cells, converting a drug-resistant phenotype to a sensitive phenotype. Menadiol is used in research related to lymphoid tumors. | ||||||||||||||||||||
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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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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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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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