1,2,3,9-TETRAHYDRO-9-METHTYL-3-METHYLENE-4H-CARBAZOL-4-ONE - Names and Identifiers
Name | 1,2,3,9-TETRAHYDRO-9-METHYL-3-METHYLENE-4H-CARBAZOL-4-ONE
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Synonyms | Ondansetron EP Impurity D Ondansetron impurity D (PhEur) Ondansetron Related Compound D (USP) 1,2,3,9-TETRAHYDRO-9-METHYL-3-METHYLENE-4H-CARBAZOL-4-ONE 9-Methyl-3-methylene-1,2,3,9-tetrahydro-4H-carbazol-4-one 1,2,3,4-TETRAHYDRO-9-METHYL-3-METHYLENE-9H-CARBAZOL-4-ONE 1,2,3,9-TETRAHYDRO-9-METHTYL-3-METHYLENE-4H-CARBAZOL-4-ONE 4H-Carbazol-4-one,1,2,3,9-tetrahydro-9-Methyl-3-Methylene- 9-methyl-3-methylidene-1,2,3,9-tetrahydro-4H-carbazol-4-one
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CAS | 99614-64-9
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InChI | InChI=1/C14H13NO/c1-9-7-8-12-13(14(9)16)10-5-3-4-6-11(10)15(12)2/h3-6H,1,7-8H2,2H3 |
1,2,3,9-TETRAHYDRO-9-METHTYL-3-METHYLENE-4H-CARBAZOL-4-ONE - Physico-chemical Properties
Molecular Formula | C14H13NO
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Molar Mass | 211.26 |
Density | 1.18 |
Boling Point | 394℃ |
Flash Point | 192℃ |
Vapor Presure | 0mmHg at 25°C |
Appearance | neat |
BRN | 7920329 |
Storage Condition | 2-8°C |
Refractive Index | 1.633 |
1,2,3,9-TETRAHYDRO-9-METHTYL-3-METHYLENE-4H-CARBAZOL-4-ONE - Risk and Safety
Hazard Symbols | T - Toxic
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Risk Codes | R25 - Toxic if swallowed
R43 - May cause sensitization by skin contact
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Safety Description | S36/37 - Wear suitable protective clothing and gloves.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
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UN IDs | UN 2811 6.1 / PGIII |
WGK Germany | 3 |
1,2,3,9-TETRAHYDRO-9-METHTYL-3-METHYLENE-4H-CARBAZOL-4-ONE - Introduction
1,2,3, is an organic compound with the chemical formula C14H15NO, also known as THMC. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
1,2,3, is a white crystalline solid that can be dissolved in some organic solvents such as methanol, ethanol and chloroform at room temperature. It has medium to high viscosity and quasi-neutral properties.
Use:
This compound is often used as an intermediate in organic synthesis and can be used to synthesize other organic compounds. It has potential application value in the field of drugs and pesticides. Due to the particularity of its structure, it can be used to synthesize biologically active molecules.
Preparation Method:
A general preparation method is to prepare 1,2,3 by hydrogenation reduction. The specific synthetic route may vary, but a common approach is to react the appropriate precursor compound with a suitable reducing agent, such as hydrogenation using hydrogen and a catalyst.
Safety Information:
Due to limited detailed studies on the safety and toxicity of this compound, it must be handled and handled with care. 1,2,3, Keep away from sources of fire and avoid contact with skin and eyes. When operating, it is recommended to wear appropriate personal protective equipment, such as laboratory gloves and eye protection. For any information on the further use and disposal of the compound, reference should be made to the relevant safety data sheets and applicable regulations.
Last Update:2024-04-09 21:04:16