2-Ethyl-benzo[d][1,3]oxazin-4-one
2-Ethyl-benzo[d][1,3]oxazin-4-one
CAS: 2916-09-8
Molecular Formula: C10H9NO2
2-Ethyl-benzo[d][1,3]oxazin-4-one - Names and Identifiers
| Name | 2-Ethyl-benzo[d][1,3]oxazin-4-one |
| Synonyms | 2-ethyl-4H-3,1-benzoxazin-4-one 2-Ethyl-benzo[d][1,3]oxazin-4-one 4H-3,1-Benzoxazin-4-one, 2-ethyl- 2-Ethyl-4H-benzo[d][1,3]oxazin-4-one |
| CAS | 2916-09-8 |
2-Ethyl-benzo[d][1,3]oxazin-4-one - Physico-chemical Properties
| Molecular Formula | C10H9NO2 |
| Molar Mass | 175.1887 |
| Storage Condition | 2-8℃ |
2-Ethyl-benzo[d][1,3]oxazin-4-one - Risk and Safety
| HS Code | 29349990 |
2-Ethyl-benzo[d][1,3]oxazin-4-one - Upstream Downstream Industry
| Downstream Products | 2-ethylquinazolin-4-ol |
2-Ethyl-benzo[d][1,3]oxazin-4-one - Introduction
2-Ethyl-benzo[d][1,3]oxazin-4-one is an organic compound with the chemical formula C12H11NO2 and a molecular weight of 205.22g/mol. It is a white crystalline solid with a special aromatic odor.
The main use of this compound is as an intermediate in organic synthesis. It can be used as a starting material for drug synthesis, dye synthesis, and other organic synthesis reactions.
The preparation of 2-Ethyl-benzo[d][1,3]oxazin-4-one is generally accomplished in a two-step reaction. The first step is a substitution reaction of benzo [D][1,3] oxazinone with ethyl bromide to form 2-ethyl-benzo [D][1,3] oxazine. The second step is the reaction of 2-Ethyl-benzo [D][1,3] oxazine with acetic anhydride to give the final product 2-Ethyl-benzo[d][1,3]oxazin-4-one.
For safety information, 2-Ethyl-benzo[d][1,3]oxazin-4-one has limited specific toxicity data and therefore needs to be handled with care. During use, general laboratory safety measures should be taken, such as wearing appropriate personal protective equipment (such as gloves and goggles). In addition, direct contact with skin and eyes should be avoided, and the compound should be stored and handled properly.
The main use of this compound is as an intermediate in organic synthesis. It can be used as a starting material for drug synthesis, dye synthesis, and other organic synthesis reactions.
The preparation of 2-Ethyl-benzo[d][1,3]oxazin-4-one is generally accomplished in a two-step reaction. The first step is a substitution reaction of benzo [D][1,3] oxazinone with ethyl bromide to form 2-ethyl-benzo [D][1,3] oxazine. The second step is the reaction of 2-Ethyl-benzo [D][1,3] oxazine with acetic anhydride to give the final product 2-Ethyl-benzo[d][1,3]oxazin-4-one.
For safety information, 2-Ethyl-benzo[d][1,3]oxazin-4-one has limited specific toxicity data and therefore needs to be handled with care. During use, general laboratory safety measures should be taken, such as wearing appropriate personal protective equipment (such as gloves and goggles). In addition, direct contact with skin and eyes should be avoided, and the compound should be stored and handled properly.
Last Update：2024-04-09 20:52:54
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CAS: 2916-09-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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Downstream Products for 2-Ethyl-benzo[d][1,3]oxazin-4-one