![]() 2-Anthraquinonecarboxylic acid structure
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Common Name | 2-Anthraquinonecarboxylic acid | ||
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CAS Number | 117-78-2 | Molecular Weight | 252.222 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 518.3±39.0 °C at 760 mmHg | |
Molecular Formula | C15H8O4 | Melting Point | 287-289 | |
MSDS | Chinese USA | Flash Point | 281.3±23.6 °C |
Use of 2-Anthraquinonecarboxylic acidAnthraquinone-2-carboxylic acid is a major anthraquinone isolated from Brazilian taheebo, with anti-inflammatory activity and antinociceptive[1]. |
Name | anthraquinone-2-carboxylic acid |
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Synonym | More Synonyms |
Description | Anthraquinone-2-carboxylic acid is a major anthraquinone isolated from Brazilian taheebo, with anti-inflammatory activity and antinociceptive[1]. |
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Related Catalog | |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 518.3±39.0 °C at 760 mmHg |
Melting Point | 287-289 |
Molecular Formula | C15H8O4 |
Molecular Weight | 252.222 |
Flash Point | 281.3±23.6 °C |
Exact Mass | 252.042252 |
PSA | 71.44000 |
LogP | 3.06 |
Vapour Pressure | 0.0±1.4 mmHg at 25°C |
Index of Refraction | 1.690 |
Stability | Stable. Incompatible with strong oxidizing agents. |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
RIDADR | NONH for all modes of transport |
HS Code | 2918300090 |
Precursor 9 | |
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DownStream 9 | |
HS Code | 2918300090 |
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Summary | 2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% |
Detecting multiple cell-secreted cytokines from the same aptamer-functionalized electrode.
Biosens. Bioelectron. 64 , 43-50, (2014) Inflammatory cytokines are secreted by immune cells in response to infection or injury. Quantification of multiple cytokines in parallel may help with disease diagnosis by illuminating inflammatory pa... |
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Adsorption state and morphology of anthraquinone-2-carboxylic acid deposited from solution onto the atomically-smooth native oxide surface of Al(111) films studied by infrared reflection absorption spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy.
Anal. Sci. 24(3) , 313-20, (2008) The adsorption state and morphology of anthraquinone-2-carboxylic acid (AQ-2-COOH) deposited from acetone solutions (0.02 - 1.00 mg ml(-1)) onto atomically-smooth native oxide surfaces of Al(111) film... |
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Prolidase as a prodrug converting enzyme. II. Synthesis of proline analogue of anthraquinone-2-carboxylic acid and its susceptibility to the action of prolidase.
Rocz. Akad. Med. Bialymst. 43 , 201-9, (1998) The feasibility to targeting prolidase as an antineoplastic prodrug--converting enzyme has been examined. The synthesis of proline analogue of anthraquinone-2-carboxylic acid (potential antineoplastic... |
9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid |
Anthraquinone-2-Carboxylic Acid |
2-Anthracenecarboxylic acid, 9,10-dihydro-9,10-dioxo- |
9,10-dioxoanthracene-2-carboxylic acid |
MFCD00001231 |
EINECS 204-207-9 |
9,10-Dioxo-9,10-dihydro-2-anthracenecarboxylic acid |