≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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.
Thiosemicarbazone derived from 5,6-dimethoxy-1-indanone inhibits bovine viral diarrhea virus infection.
5,6-Dimethoxy-1-indanone was used in the synthesis of 2,3-dimethoxy-11H-indeno1,2-bquinoline-6,10-dicarboxylic acid.
| Pubchem Sid | 488185015 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488185015 |
| Sonrisas canónicas | COC1=C(C=C2C(=C1)CCC2=O)OC |
| IUPAC Name | 5,6-dimethoxy-2,3-dihydroinden-1-one |
| InChIKey | IHMQOBPGHZFGLC-UHFFFAOYSA-N |
| INCHI | 1S/C11H12O3/c1-13-10-5-7-3-4-9(12)8(7)6-11(10)14-2/h5-6H,3-4H2,1-2H3 |
| Isómeros SMILES | COC1=C(C=C2C(=C1)CCC2=O)OC |
| WGK Alemania | 3 |
| Peso molecular | 192.21 |
| Beilstein | 1241095 |
| Reaxy-Rn | 1241095 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1241095&ln= |
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 |
| Clase | Indanes |
| Subclass | Indanones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indanones |
| Alternative Parents | Aryl alkyl ketones Anisoles Alkyl aryl ethers Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Indanone - Aryl alkyl ketone - Aryl ketone - Anisole - Alkyl aryl ether - Ketone - Ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as indanones. These are compounds containing an indane ring bearing a ketone group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 J2129477 | Certificate of Analysis | Aug 11, 2025 | D101913 |
| J2129508 | Certificate of Analysis | Aug 11, 2025 | D101913 |
| G1204051 | Certificate of Analysis | Feb 08, 2025 | D101913 |
| A2607317 | Certificate of Analysis | Jul 18, 2024 | D101913 |
| D2410208 | Certificate of Analysis | Mar 21, 2024 | D101913 |
| D2423517 | Certificate of Analysis | Mar 21, 2024 | D101913 |
| I2502052 | Certificate of Analysis | Mar 21, 2024 | D101913 |
| C2330929 | Certificate of Analysis | May 22, 2021 | D101913 |
| K2429066 | Certificate of Analysis | May 22, 2021 | D101913 |
| Solubilidad | Soluble in Methanol |
|---|---|
| Punto de ebullición (°C) | 139°C/2mmHg |
| Punto de fusión (°C) | 118-120°C |
| Peso molecular | 192.210 g/mol |
| XLogP3 | 1.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 192.079 Da |
| Monoisotopic Mass | 192.079 Da |
| Topological Polar Surface Area | 35.500 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 227.000 |
| 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 |
