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| Synonyms | Tricarbonyl(methyl benzoate)chromium;Methyl benchrotrene carboxylate;METHYLBENZOATE CHROMIUM TRICARBONYL;Benzoic acid, methyl ester, chromium tricarbonyl complex |
| Molecular Formula | C11H8CrO56* |
| Molecular Weight | 272.17 |
| Melting Point | 95-96°C |
| Sensibility | Air & moisture sensitive |
| Purity | ≧ 98% |
| Package Information | 100g, 500g, 1kg, or customized |
The methyl benzoate aromatic ring forms an η⁶-π coordination with Cr(CO)₃, which allows the molecule to maintain good structural stability under conventional experimental conditions, making it suitable for subsequent reaction studies.
The electron-withdrawing properties of Cr(CO)3 can significantly alter the electron distribution of the aromatic ring, leading to unique reactivity of the aromatic system in electrophilic or selective reactions.
These types of complexes are commonly used to study the activation and directed substitution of aromatic compounds, as well as reaction pathways involving transition metals.
Suitable for laboratory-scale synthesis and customized requirements, facilitating the development of novel aromatic complexes or derivatives.
(Methyl Benzoate) Tricarbonyl Chromium is commonly used to study the changes in electronic structure and reaction behavior of aromatic esters under metal coordination conditions.
Coordination with Cr(CO)3 can alter the reaction site of the aromatic ring, which can be used to explore regioselective substitution, addition, or rearrangement reactions.
As one of the classic tricarbonyl chromium aromatic complexes, it is widely used in teaching experiments and mechanism verification in universities and research institutions.
This compound can be used as a starting material for further modification or derivatization reactions, for the development of functionalized aromatic metal complexes.
Prolonged exposure to light should be avoided, as light can induce the dissociation of carbonyl ligands, affecting the product's structure and purity.
The moisture and oxygen in the air can cause the metal center to oxidize slowly; therefore, it should be stored in a sealed container to prevent air and moisture from entering.
High temperatures may cause CO ligands to desorb, posing a safety hazard, so extra caution is needed.
It is recommended to wear gloves and safety glasses during operation, and to perform the procedure in a fume hood or under an inert atmosphere.
Waste liquids and residues must be disposed of properly in accordance with regulations concerning organometallic compounds; indiscriminate dumping is prohibited.
1. What type of compound is (Methyl Benzoate) Tricarbonyl Chromium? What are its application areas?
It is an organometallic complex of tricarbonyl chromium coordinated with an aromatic ester, belonging to the Cr(0) organometallic chemistry system. This compound is primarily used in organometallic chemistry, studies of reaction mechanisms of aromatic compounds, and custom synthesis.
2. Is this compound sensitive to air or light?
Yes, it is recommended to store and handle it under light-protected, dry, and inert atmosphere conditions.
3. Can you provide MSDS and COA?
Yes, we typically provide MSDS, COA, and other technical documents with the shipment or upon request.
4. Do you support bulk or customized specifications?
We support both research scale and bulk orders, and can customize purity and packaging specifications according to your needs.
Wolfa professionally supplies (Methyl 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 | Tricarbonyl(methyl benzoate)chromium;Methyl benchrotrene carboxylate;METHYLBENZOATE CHROMIUM TRICARBONYL;Benzoic acid, methyl ester, chromium tricarbonyl complex |
| Molecular Formula | C11H8CrO56* |
| Molecular Weight | 272.17 |
| Melting Point | 95-96°C |
| Sensibility | Air & moisture sensitive |
| Purity | ≧ 98% |
| Package Information | 100g, 500g, 1kg, or customized |
The methyl benzoate aromatic ring forms an η⁶-π coordination with Cr(CO)₃, which allows the molecule to maintain good structural stability under conventional experimental conditions, making it suitable for subsequent reaction studies.
The electron-withdrawing properties of Cr(CO)3 can significantly alter the electron distribution of the aromatic ring, leading to unique reactivity of the aromatic system in electrophilic or selective reactions.
These types of complexes are commonly used to study the activation and directed substitution of aromatic compounds, as well as reaction pathways involving transition metals.
Suitable for laboratory-scale synthesis and customized requirements, facilitating the development of novel aromatic complexes or derivatives.
(Methyl Benzoate) Tricarbonyl Chromium is commonly used to study the changes in electronic structure and reaction behavior of aromatic esters under metal coordination conditions.
Coordination with Cr(CO)3 can alter the reaction site of the aromatic ring, which can be used to explore regioselective substitution, addition, or rearrangement reactions.
As one of the classic tricarbonyl chromium aromatic complexes, it is widely used in teaching experiments and mechanism verification in universities and research institutions.
This compound can be used as a starting material for further modification or derivatization reactions, for the development of functionalized aromatic metal complexes.
Prolonged exposure to light should be avoided, as light can induce the dissociation of carbonyl ligands, affecting the product's structure and purity.
The moisture and oxygen in the air can cause the metal center to oxidize slowly; therefore, it should be stored in a sealed container to prevent air and moisture from entering.
High temperatures may cause CO ligands to desorb, posing a safety hazard, so extra caution is needed.
It is recommended to wear gloves and safety glasses during operation, and to perform the procedure in a fume hood or under an inert atmosphere.
Waste liquids and residues must be disposed of properly in accordance with regulations concerning organometallic compounds; indiscriminate dumping is prohibited.
1. What type of compound is (Methyl Benzoate) Tricarbonyl Chromium? What are its application areas?
It is an organometallic complex of tricarbonyl chromium coordinated with an aromatic ester, belonging to the Cr(0) organometallic chemistry system. This compound is primarily used in organometallic chemistry, studies of reaction mechanisms of aromatic compounds, and custom synthesis.
2. Is this compound sensitive to air or light?
Yes, it is recommended to store and handle it under light-protected, dry, and inert atmosphere conditions.
3. Can you provide MSDS and COA?
Yes, we typically provide MSDS, COA, and other technical documents with the shipment or upon request.
4. Do you support bulk or customized specifications?
We support both research scale and bulk orders, and can customize purity and packaging specifications according to your needs.
Wolfa professionally supplies (Methyl 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.
