32499-64-2
N-Carbethoxy-4-tropinone
CAS: 32499-64-2
Molecular Formula: C10H15NO3
32499-64-2 - Names and Identifiers
| Name | N-Carbethoxy-4-tropinone |
| Synonyms | n-(carboethoxy)tropinone N-Carbethoxy-4-tropinone N-Carbethoxy-4-nortropinone N-(Ethoxycarbonyl)nortropinone N-(ETHOXYCAZBONYL)NORTROPINONE N-ethoxycarbonylnortropan-3-one 3-Oxo-8-azabicylo[3.2.1]octane-8-carboxylic acid ethyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylate N-(Carboethoxy)tropinone~3-Oxo-8-azabicyclo[3.2.1]octane-8-carboxylic acid ethyl ester |
| CAS | 32499-64-2 |
| EINECS | 1312995-182-4 |
| InChI | InChI=1/C10H15NO3/c1-2-14-10(13)11-7-3-4-8(11)6-9(12)5-7/h7-8H,2-6H2,1H3 |
32499-64-2 - Physico-chemical Properties
| Molecular Formula | C10H15NO3 |
| Molar Mass | 197.23 |
| Density | 1.1575 (rough estimate) |
| Boling Point | 152-153°C 11mm |
| Flash Point | 152-153°C/11mm |
| Vapor Presure | 0.00057mmHg at 25°C |
| Appearance | Liquid |
| Color | Clear slightly yellow to light brown |
| BRN | 1530944 |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.4876-1.4896 |
| MDL | MFCD00078171 |
32499-64-2 - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| HS Code | 29399990 |
32499-64-2 - Introduction
N-Carbethoxy-4-tropinone(N-Carbethoxy-4-tropinone) is an organic compound whose molecular formula is C11H15NO3. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
N-Carbethoxy-4-tropinone is a solid with a white or light yellow crystalline form. It can be dissolved in some organic solvents, such as chloroform and ethanol. The melting point of the compound is about 130-135 degrees Celsius.
Use:
N-Carbethoxy-4-tropinone is often used as an intermediate in organic synthesis. It can be used to synthesize other organic compounds, especially for the synthesis of dominant amides and anhydrides. In addition, it can also be used as a precursor for the synthesis of drugs, natural products and other organic synthesis reactions.
Method:
N-Carbethoxy-4-tropinone can be prepared in a variety of ways. The most common method is obtained by acylation of sodium hydrogen acetate in solution with opsonins. Other methods include alkylation of opsonins using alkylating agents and subsequent carboxylation reactions.
Safety Information:
Information on N-Carbethoxy-4-tropinone safety is currently limited. As an organic compound, it may have some irritation and toxicity. When handling or using the compound, follow safe practices, including wearing protective gloves, glasses, and a protective mask, and avoid inhalation, ingestion, or contact with skin. In addition, it should be operated in a well-ventilated area to prevent evaporation of the compound. If the compound is intentionally touched or ingested, seek medical attention immediately. When used in the laboratory, the relevant safe operation guidelines should be followed and the waste should be disposed of correctly. In order to ensure safety, it is recommended to handle and handle the compound under the guidance of professionals.
Nature:
N-Carbethoxy-4-tropinone is a solid with a white or light yellow crystalline form. It can be dissolved in some organic solvents, such as chloroform and ethanol. The melting point of the compound is about 130-135 degrees Celsius.
Use:
N-Carbethoxy-4-tropinone is often used as an intermediate in organic synthesis. It can be used to synthesize other organic compounds, especially for the synthesis of dominant amides and anhydrides. In addition, it can also be used as a precursor for the synthesis of drugs, natural products and other organic synthesis reactions.
Method:
N-Carbethoxy-4-tropinone can be prepared in a variety of ways. The most common method is obtained by acylation of sodium hydrogen acetate in solution with opsonins. Other methods include alkylation of opsonins using alkylating agents and subsequent carboxylation reactions.
Safety Information:
Information on N-Carbethoxy-4-tropinone safety is currently limited. As an organic compound, it may have some irritation and toxicity. When handling or using the compound, follow safe practices, including wearing protective gloves, glasses, and a protective mask, and avoid inhalation, ingestion, or contact with skin. In addition, it should be operated in a well-ventilated area to prevent evaporation of the compound. If the compound is intentionally touched or ingested, seek medical attention immediately. When used in the laboratory, the relevant safe operation guidelines should be followed and the waste should be disposed of correctly. In order to ensure safety, it is recommended to handle and handle the compound under the guidance of professionals.
Last Update：2024-04-09 21:54:55
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