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Basic Description
| Synonyms | NSC 22835 | 2-Hydroxy-9-fluorenone, 98% | AS-58713 | H0329 | 2-Hydroxy-9H-fluoren-9-one | DTXSID00219716 | 2-hydroxy-fluoren-9-one | 2-Hydroxyfluoren-9-one | DR37FXR63Q | Z1255485150 | NSC22835 | NSC-22835 | MFCD00001155 | 9H-Fluoren-9-one, 2-hydroxy- | S |
|---|---|
| Specifications & Purity | ≥98% |
| Shipped In | Normal |
| Product Description |
Reactant involved in: 1.One-pot synthesis of aryl substituted aurones. 2.Studies to tune HOMO-LUMO levels of 9-fluorenone scaffolds. 3.O-methylation for synthesis of second-generation light driven rotary molecular motors. 4.Reactions with aluminum, gallium compounds, and methylquinolines. 5. Synthesis of acridinyl- and fluorenylidenehydrazido calixarenes. 6.Acetylation for synthesis of acetates. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
- Class Fluorenes
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Superclass
Benzenoids
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Fluorenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fluorenes |
| Alternative Parents | Aryl ketones 1-hydroxy-2-unsubstituted benzenoids Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Fluorene - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene. |
| External Descriptors | Not available |
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Associated Targets(Human)
A498 (42825 Activities)
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CAKI-1 (44928 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCT-116 (91556 Activities)
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Hs-578T (29457 Activities)
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LOX IMVI (44321 Activities)
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HOP-62 (47048 Activities)
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MDA-MB-435 (38290 Activities)
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Malme-3M (44254 Activities)
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MDA-MB-231 (73002 Activities)
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SNB-75 (44215 Activities)
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NCI-H226 (44470 Activities)
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NCI-H23 (49055 Activities)
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NCI-H522 (44358 Activities)
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SF-539 (44845 Activities)
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Names and Identifiers
| Pubchem Sid | 488185957 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488185957 |
| IUPAC Name | 2-hydroxyfluoren-9-one |
| INCHI | InChI=1S/C13H8O2/c14-8-5-6-10-9-3-1-2-4-11(9)13(15)12(10)7-8/h1-7,14H |
| InChIKey | GXUBPHMYNSICJC-UHFFFAOYSA-N |
| Smiles | C1=CC=C2C(=C1)C3=C(C2=O)C=C(C=C3)O |
| Isomeric SMILES | C1=CC=C2C(=C1)C3=C(C2=O)C=C(C=C3)O |
| WGK Germany | 3 |
| Molecular Weight | 196.2 |
| Beilstein | 8188 |
| Reaxy-Rn | 1871045 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1871045&ln= |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 G2307362 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307376 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307363 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307356 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307636 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307635 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307361 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| G2307377 |
Certificate of Analysis | Jun 15, 2023 | H121522 |
| L1812139 |
Certificate of Analysis | Oct 17, 2022 | H121522 |
| D2314516 |
Certificate of Analysis | Oct 17, 2022 | H121522 |
Chemical and Physical Properties
| Solubility | Soluble in Acetone |
|---|---|
| Melt Point(°C) | 204-206°C |
| Molecular Weight | 196.200 g/mol |
| XLogP3 | 3.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 196.052 Da |
| Monoisotopic Mass | 196.052 Da |
| Topological Polar Surface Area | 37.300 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 274.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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