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| Synonyms | (ETHYL BENZOATE)TRICARBONYLCHROMIUM;(ethyl benzoate)tricarbonyl chromium(0);(Ethylbenzoate)chromium tricarbonyl;(Benzoic acid)chromium tricarbonyl ethyl ester |
| Molecular Formula | C12H10CrO5 |
| Appearance | Powder |
| Molecular Weight | 286.2 |
| Melting Point | 54-59 °C(lit.) |
| Flash Point | >230 °F |
| Sensibility | Air & moisture sensitive |
| Purity | ≧ 98% |
| Package Information | 100g, 500g, 1kg, or customized |
Ethyl benzoate, with its aromatic ring coordinated to Cr(CO)3 in an η⁶ fashion, is a representative system for studying aromatic π-complexation effects.
Coordination with Cr(CO)3 reduces the electron density of the aromatic ring, making it uniquely valuable in electrophilic or directed reaction studies.
The structure is stable under light-shielded and inert conditions, and its spectral characteristics are well-defined, making it suitable for scientific experiments requiring high reproducibility.
(Ethyl benzoate)tricarbonyl chromium is often used as a model for aromatic π-complexes to study the interaction between chromium carbonyl and aromatic systems.
Through coordination with Cr(CO)3, the behavioral changes of aromatic esters in electrophilic substitution and regioselective reactions can be systematically studied.
This involves developing and validating new methods for the functionalization of aromatic compounds, particularly in metal-catalyzed reaction systems.
Exposure to light may lead to the gradual dissociation of Cr–aromatic coordination bonds, affecting the stability of the compound; therefore, prolonged exposure to light should be avoided.
Exposure to air and moisture may cause slow decomposition; therefore, it is recommended to perform the operation under an inert atmosphere or under rapid conditions.
Carbon monoxide (CO) may be released under high-temperature conditions; therefore, the experiment should be conducted in a well-ventilated laboratory environment.
1. What are the main uses of (ethyl benzoate)tricarbonylchromium?
It is mainly used in organometallic chemistry, aromatic reactivity control, and mechanistic studies.
2. Is this product suitable for industrial production?
It is primarily for research purposes and is not intended for use as a direct industrial raw material.
3. Does this compound require specific storage conditions?
Yes, it needs to be stored away from light, in a sealed container, at a low temperature, and preferably under an inert atmosphere.
Wolfa professionally supplies (Ethyl Benzoate) Tricarbonyl Chromium, supporting small-batch sampling and large-volume procurement needs. Packaging options include ordinary glass bottles, glass ampoules, metal ampoules, etc.
For product analysis reports (such as COA) or procurement consulting, please feel free to contact us at jomin@wolfabio.com at any time.
| Synonyms | (ETHYL BENZOATE)TRICARBONYLCHROMIUM;(ethyl benzoate)tricarbonyl chromium(0);(Ethylbenzoate)chromium tricarbonyl;(Benzoic acid)chromium tricarbonyl ethyl ester |
| Molecular Formula | C12H10CrO5 |
| Appearance | Powder |
| Molecular Weight | 286.2 |
| Melting Point | 54-59 °C(lit.) |
| Flash Point | >230 °F |
| Sensibility | Air & moisture sensitive |
| Purity | ≧ 98% |
| Package Information | 100g, 500g, 1kg, or customized |
Ethyl benzoate, with its aromatic ring coordinated to Cr(CO)3 in an η⁶ fashion, is a representative system for studying aromatic π-complexation effects.
Coordination with Cr(CO)3 reduces the electron density of the aromatic ring, making it uniquely valuable in electrophilic or directed reaction studies.
The structure is stable under light-shielded and inert conditions, and its spectral characteristics are well-defined, making it suitable for scientific experiments requiring high reproducibility.
(Ethyl benzoate)tricarbonyl chromium is often used as a model for aromatic π-complexes to study the interaction between chromium carbonyl and aromatic systems.
Through coordination with Cr(CO)3, the behavioral changes of aromatic esters in electrophilic substitution and regioselective reactions can be systematically studied.
This involves developing and validating new methods for the functionalization of aromatic compounds, particularly in metal-catalyzed reaction systems.
Exposure to light may lead to the gradual dissociation of Cr–aromatic coordination bonds, affecting the stability of the compound; therefore, prolonged exposure to light should be avoided.
Exposure to air and moisture may cause slow decomposition; therefore, it is recommended to perform the operation under an inert atmosphere or under rapid conditions.
Carbon monoxide (CO) may be released under high-temperature conditions; therefore, the experiment should be conducted in a well-ventilated laboratory environment.
1. What are the main uses of (ethyl benzoate)tricarbonylchromium?
It is mainly used in organometallic chemistry, aromatic reactivity control, and mechanistic studies.
2. Is this product suitable for industrial production?
It is primarily for research purposes and is not intended for use as a direct industrial raw material.
3. Does this compound require specific storage conditions?
Yes, it needs to be stored away from light, in a sealed container, at a low temperature, and preferably under an inert atmosphere.
Wolfa professionally supplies (Ethyl Benzoate) Tricarbonyl Chromium, supporting small-batch sampling and large-volume procurement needs. Packaging options include ordinary glass bottles, glass ampoules, metal ampoules, etc.
For product analysis reports (such as COA) or procurement consulting, please feel free to contact us at jomin@wolfabio.com at any time.
