Chemodex

2,3-Dihydroxy-naphthalin

CHF 116.00
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CDX-D0892-G100100 gCHF 116.00
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Product Details
Synonyms 2,3-DHN; 2,3-Naphthalenediol; 2,3-Dihydroxy-naphthalin; 2,3-Naphthalindiol
Product Type Chemical
Properties
Formula C10H8O2
MW 160.17
CAS 92-44-4
RTECS QJ4750000
Purity Chemicals ≥98% (HPLC)
Appearance White to faint beige powder or crystals.
Solubility Soluble in DMSO or methanol (1mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key JRNGUTKWMSBIBF-UHFFFAOYSA-N
Smiles Oc1cc2ccccc2cc1O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Keep under inert gas.
Very hygroscopic.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

2,3-Dihydroxynaphthalene (2,3-DHN) is a naturally occurring catechol. 2,3-Dihydroxynaphthalene (2,3-DHN) can be used as a building block, starting material or reagent in organic synthesis to create more complex chemical compounds. The hydroxyl groups in 2,3-DHN can undergo various chemical reactions, such as esterification, oxidation, or substitution reactions, to produce a wide range of derivatives. 2,3-Dihydroxynaphthalene displays the ability to function as either an electron donor or acceptor in redox reactions. It also serves as an electron transfer agent in enzymatic reactions. 2,3-DHN and its derivatives can be used in the synthesis of dyes and pigments. 2,3-DHN and its derivatives have been shown to inhibit certain enzymes and have potential anti-tumor properties. 2,3-DHN is a metal chelators.

Product References

(1) J.C. DiNardo, et al.; Toxicol. Appl. Pharmacol. 78, 163 (1985) | (2) P.K. Tarafder, et al.; Talanta 41, 1345 (1994) | (3) R. Shiman, et al.; J. Cell Biol. 236, 24637 (1994) | (4) S. Bhownik & U. Maitra; Chem. Commun. 48, 4624 (2012) | (5) J. Feng, et al.; Dalton Trans. 41, 8697 (2012) | (6) L.M. Laglera, et al.; Anal. Chem. 85, 2486 (2013) | (7) M. Burton, et al.; Bioorg. Med. Chem. 26, 4841 (2018)

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