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.
Indium(III) Isopropoxide is an organo-metallic compound. Indium(III) Isopropoxide uesd as a hydrogen transfer catalyst for conversion of benzylic alcohols into aldehydes or ketones via Oppenauer oxidation. Indium(III) Isopropoxide also can be used as metal precursor.
In Vitro
Indium(III) isopropoxide as an Oppenaueroxidation catalyst, and the conversion of primary or secondary alcohols into the corresponding aldehydes or ketones was promoted at room temperature using pivalaldehyde as an oxidant. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Form:Solid
| Sonrisas canónicas | CC(C)[O-].CC(C)[O-].CC(C)[O-].[In+3] |
|---|---|
| IUPAC Name | indium(3+);propan-2-olate |
| InChIKey | OVZUSPADPSOQQN-UHFFFAOYSA-N |
| INCHI | 1S/3C3H7O.In/c3*1-3(2)4;/h3*3H,1-2H3;/q3*-1;+3 |
| Isómeros SMILES | CC(C)[O-].CC(C)[O-].CC(C)[O-].[In+3] |
| CAS alternativo | 118240-53-2,38218-24-5 |
| PubChem CID | 57346963 |
| Peso molecular | 97.36 |
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 | Organic oxygen compounds |
| Clase | Organic oxides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organic oxides |
| Alternative Parents | Organic zwitterions Organic salts Hydrocarbon derivatives Alkoxides |
| Molecular Framework | Not available |
| Substituents | Organic oxide - Hydrocarbon derivative - Organic salt - Organic zwitterion - Alkoxide - Organooxygen compound - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as organic oxides. These are organic compounds containing an oxide group. |
| External Descriptors | Not available |
| Solubilidad | H2O : <0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) DMSO : <1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble or slightly soluble) |
|---|---|
| Peso molecular | 292.080 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 292.053 Da |
| Monoisotopic Mass | 292.053 Da |
| Topological Polar Surface Area | 69.200 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 10.800 |
| 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 | 4 |
