≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Sulindac Sulfide is a potent γ-secretase modulator (GSM).Sulindac Sulfide selectively reduces Aβ42 production in favor of shorter Aβ species. Sulindac Sulfide can be used for researching Alzheimer’s disease.
| Pubchem Sid | 504763992 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504763992 |
| Canonical Smiles | CC1=C(C2=C(C1=CC3=CC=C(C=C3)SC)C=CC(=C2)F)CC(=O)O |
| IUPAC Name | 2-[(3E)-6-fluoro-2-methyl-3-[(4-methylsulfanylphenyl)methylidene]inden-1-yl]acetic acid |
| InChIKey | LFWHFZJPXXOYNR-RQZCQDPDSA-N |
| INCHI | 1S/C20H17FO2S/c1-12-17(9-13-3-6-15(24-2)7-4-13)16-8-5-14(21)10-19(16)18(12)11-20(22)23/h3-10H,11H2,1-2H3,(H,22,23)/b17-9+ |
| Isomeric SMILES | CC\1=C(C2=C(/C1=C/C3=CC=C(C=C3)SC)C=CC(=C2)F)CC(=O)O |
| WGK Germany | 3 |
| PubChem CID | 6034911 |
| Molecular Weight | 340.41 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Indenes and isoindenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indenes and isoindenes |
| Alternative Parents | Thiophenol ethers Alkylarylthioethers Benzene and substituted derivatives Aryl fluorides Sulfenyl compounds Monocarboxylic acids and derivatives Carboxylic acids Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Indene - Aryl thioether - Thiophenol ether - Alkylarylthioether - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Sulfenyl compound - Thioether - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organofluoride - Organohalogen compound - Carbonyl group - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as indenes and isoindenes. These are compounds containing an indene moiety(which consists of a cyclopentadiene fused to a benzene ring), or a isoindene moiety (which consists of a cyclopentadiene fused to cyclohexadiene ring). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 H2321031 | Certificate of Analysis | Jul 31, 2023 | S160989 |
| H2321032 | Certificate of Analysis | Jul 31, 2023 | S160989 |
| H2321033 | Certificate of Analysis | Jul 31, 2023 | S160989 |
| H2321072 | Certificate of Analysis | Jul 31, 2023 | S160989 |
| H2321073 | Certificate of Analysis | Jul 31, 2023 | S160989 |
| H2321074 | Certificate of Analysis | Jul 31, 2023 | S160989 |
| Sensitivity | Heat sensitive；Hygroscopic |
|---|---|
| Melt Point(°C) | 186 °C |
| Molecular Weight | 340.400 g/mol |
| XLogP3 | 4.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 340.093 Da |
| Monoisotopic Mass | 340.093 Da |
| Topological Polar Surface Area | 62.600 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 546.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
