138999-35-6Oc1cccc2cccc(O)c12OENHRRVNRZBNNS-UHFFFAOYSA-NNaphthalene-1,8-diol is a member of the class of naphthalenediols that is naphthalene in which the hydrogens at positions 1 and 8 are replaced by hydroxy groups. It has a role as a fungal metabolite.
138999-35-6、569-42-6DTXSID80205435CHEMBL203537CHEBI:167604化学的特性1,8-Naphthalenediol [569-42-6], mp 144℃, is produced by caustic fusion of naphthosultone or naphthosultam, and by acid desulfonation of 1,8-dihydroxynaphthalene-4-sulfonic acid. It is oxidized to juglone by chromium(VI) oxide; gives a dark green color with iron(III) chloride; undergoes amination at 300℃ to give 1,8-naphthalenediamine; and couples with diazotized anilines in the 4- position.
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Danger
H318 (97.5%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
P264+P265, P280, P305+P354+P338, and P317 (click each P-code to see the statement)
Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory.
使用1,8-Dihydroxynaphthalene (DHN) can be used as:An intermediate in the preparation of benzo analogs of spiromamakone A.A starting material to synthesize naphthopyran derivatives.An intermediate in the total synthesis of palmarumycin CP17 analogs.
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