1-羟基蒽醌（CAS 129-43-1）：分子式 C14H8O3、分子量 224.21。
| CAS号 | 129-43-1 |
|---|---|
| 分子式 | C14H8O3 |
| 分子量 | 224.21 |
| 熔点 | 193.8 °C |
| LogP | log Kow = 3.52 |
| 应用领域 | Uses: Used to make dyes and pharmaceuticals、[HSDB]、1-Hydroxyanthraquinone can be used as an intermediate in the production of dyes and drugs.、Methods of Manufacturing: A general method for synthesis of anthraquinones、including 1-hydroxy-anthraquinone、has been developed. The anthraquinones were obtained under mild conditions from ortho-dicarboxylic acid chlorides and suitable aromatic substrates via a FriedelCrafts process.、1-Hydroxyanthraquinone has been synthesized by diazotization of 1-aminoanthraquinone and heating the diazonium salt with concentrated sulfuric acid. After dilution with water、the precipitated crude product was diluted with acetone and purified by preparative thin-layer chromatography (TLC) in toluene:ethyl formate:formic acid (75:24:1).、1-Hydroxyanthraquinone has also been prepared in 96.4% yield by reacting 1-nitroanthraquinone with sodium formate in dimethylformamide at 130 C for 17 hours.、General Manufacturing Information: 9、10-Anthracenedione、1-hydroxy-: INACTIVE、1-Hydroxyanthraquinone has been isolated from the roots of Rubia cordifolia、Morinda officinalis and Damnacanthus indicus、from the heartwood of Tabebuia avellanedae and the herb Cassia occidentalis. |
登记用途：Uses: Used to make dyes and pharmaceuticals、[HSDB]、1-Hydroxyanthraquinone can be used as an intermediate in the production of dyes and drugs.、Methods of Manufacturing: A general method for synthesis of anthraquinones、including 1-hydroxy-anthraquinone、has been developed. The anthraquinones were obtained under mild conditions from ortho-dicarboxylic acid chlorides and suitable aromatic substrates via a FriedelCrafts process.、1-Hydroxyanthraquinone has been synthesized by diazotization of 1-aminoanthraquinone and heating the diazonium salt with concentrated sulfuric acid. After dilution with water、the precipitated crude product was diluted with acetone and purified by preparative thin-layer chromatography (TLC) in toluene:ethyl formate:formic acid (75:24:1).、1-Hydroxyanthraquinone has also been prepared in 96.4% yield by reacting 1-nitroanthraquinone with sodium formate in dimethylformamide at 130 C for 17 hours.、General Manufacturing Information: 9、10-Anthracenedione、1-hydroxy-: INACTIVE、1-Hydroxyanthraquinone has been isolated from the roots of Rubia cordifolia、Morinda officinalis and Damnacanthus indicus、from the heartwood of Tabebuia avellanedae and the herb Cassia occidentalis.。
1-羟基蒽醌 是一种化工化合物，登记 CAS 号为 129-43-1，分子式 C14H8O3（分子量 224.21）。
登记 CAS 号：129-43-1
其分子式 C14H8O3 由 14 个碳、8 个氢、3 个氧 组成。
别名/同义词：1-羟基蒽醌 · 1-hydroxyanthraquinone
1-羟基蒽醌 的 CAS 登记号为 129-43-1。
分子式 C14H8O3，分子量 224.21。
别名/同义词：1-羟基蒽醌、1-hydroxyanthraquinone。
登记用途：Uses: Used to make dyes and pharmaceuticals、[HSDB]、1-Hydroxyanthraquinone can be used as an intermediate in the production of dyes and drugs.、Methods of Manufacturing: A general method for synthesis of anthraquinones、including 1-hydroxy-anthraquinone、has been developed. The anthraquinones were obtained under mild conditions from ortho-dicarboxylic acid chlorides and suitable aromatic substrates via a FriedelCrafts process.、1-Hydroxyanthraquinone has been synthesized by diazotization of 1-aminoanthraquinone and heating the diazonium salt with concentrated sulfuric acid. After dilution with water、the precipitated crude product was diluted with acetone and purified by preparative thin-layer chromatography (TLC) in toluene:ethyl formate:formic acid (75:24:1).、1-Hydroxyanthraquinone has also been prepared in 96.4% yield by reacting 1-nitroanthraquinone with sodium formate in dimethylformamide at 130 C for 17 hours.、General Manufacturing Information: 9、10-Anthracenedione、1-hydroxy-: INACTIVE、1-Hydroxyanthraquinone has been isolated from the roots of Rubia cordifolia、Morinda officinalis and Damnacanthus indicus、from the heartwood of Tabebuia avellanedae and the herb Cassia occidentalis.。
1-羟基蒽醌（CAS 129-43-1）的独立参考数据，整理自公开化学数据库。
| CAS Registry Number | 129-43-1 |
|---|---|
| PubChem CID | 8512 |
| Molecular formula | C14H8O3 |
| IUPAC name | 1-hydroxyanthracene-9,10-dione |
| UNII (FDA) | LFU129OE9H |
| Molecular Weight | 224.21 |
|---|---|
| XLogP3 | 3.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 224.047344113 |
| Monoisotopic Mass | 224.047344113 |
| Topological Polar Surface Area | 54.4 |
| Heavy Atom Count | 17 |
| Melting Point | 193.8 °C |
|---|---|
| Solubility | In water, 8.5 mg/L @ 25 °C |
| Vapor Pressure | 0.00000021 [mmHg] |
| Vapor Pressure | 2.09X10-7 mm Hg @ 25 °C |
| LogP | log Kow = 3.52 |
| LogP | 3.52 |
1-HYDROXYANTHRAQUINONE; 129-43-1; 1-hydroxyanthracene-9,10-dione; 9,10-Anthracenedione, 1-hydroxy-; 1-Hydroxy-9,10-anthraquinone; Hydroxyanthraquinone; 1-Hydroxyanthrachinon; Anthraquinone, 1-hydroxy-; alpha-Hydroxyanthraquinone; LFU129OE9H; 1-hydroxy-9,10-anthracenedione; CHEBI:28877; NSC-8640; DTXSID1020722; RefChem:76013; DTXCID70722
| Reported hazard statements | H319 (100%), H351 (100%), H320 |
|---|
H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H351 (100%): Suspected of causing cancer [Warning Carcinogenicity]
1-hydroxyanthraquinone · CAS 129-43-1 · C14H8O3. UNII LFU129OE9H. Melting Point: 193.8 °C; Solubility: In water, 8.5 mg/L @ 25 °C; Vapor Pressure: 0.00000021 [mmHg].
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: 1-hydroxyanthraquinone