2882-15-7
5-Methoxy-2-methyl-3-indoleacetic acid
CAS: 2882-15-7
Molecular Formula: C12H13NO3
2882-15-7 - Names and Identifiers
| Name | 5-Methoxy-2-methyl-3-indoleacetic acid |
| Synonyms | Indomethacin USP RC A Indomethacin EP Impurity B 5-METHOXY-2-METHYL INDOLE ACETIC ACID 5-Methoxy-2-methyl-3-indoleacetic acid 5-METHOXY-2-METHYL-3-INDOLEACETIC ACID 5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID 5-methoxy-2-methylindol-3-ylacetic acid (5-methoxy-2-methyl-1H-indol-3-yl)acetate (5-methoxy-2-methyl-1H-indol-3-yl)acetic acid (5-METHOXY-2-METHYL-1H-INDOL-3-YL)-ACETIC ACID |
| CAS | 2882-15-7 |
| EINECS | 220-734-7 |
| InChI | InChI=1/C12H13NO3/c1-7-9(6-12(14)15)10-5-8(16-2)3-4-11(10)13-7/h3-5,13H,6H2,1-2H3,(H,14,15)/p-1 |
2882-15-7 - Physico-chemical Properties
| Molecular Formula | C12H13NO3 |
| Molar Mass | 219.24 |
| Density | 1.1825 (rough estimate) |
| Melting Point | 161-163 °C (lit.) |
| Boling Point | 360.05°C (rough estimate) |
| Flash Point | 226.1°C |
| Solubility | methanol: soluble |
| Vapor Presure | 6.83E-09mmHg at 25°C |
| Appearance | Solid |
| Color | Off-white to light yellow or light beige |
| pKa | 4.22±0.30(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.5270 (estimate) |
| MDL | MFCD00005618 |
2882-15-7 - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29349990 |
2882-15-7 - Introduction
Acid (acid) is an organic compound with the chemical formula C12H13NO3. It is a white or off-white crystalline solid.
This compound is mainly an auxin analog, which has the properties of a plant growth regulator. It plays a role in regulating hormones in plant growth and development. In addition, it has a broad spectrum of fungicidal activity and can be used as a fungicide in agriculture.
The acid preparation method can be carried out through the following steps:
1. Preparation of N-animal oleoyl indole by condensation of Wuskeimide and animal oleic acid;
2. N-oleoyl indole reacts with acetic anhydride to produce N-oleoyl indole acetate;
3. N-oleoyl indole acetate reacts with silver oxide to give N-oleoyl indole carboxaldehyde;
4. N-animal oleoyl indole carboxaldehyde reacts with methanol to generate chromium acid.
Regarding safety information, acid has no obvious danger under normal use conditions. However, as a chemical, appropriate laboratory safety practices should be followed, including wearing appropriate protective equipment, avoiding inhalation, skin contact and eye contact, and avoiding contact with combustibles and oxidants. In case of accidental contact or accidental ingestion, please seek medical advice immediately.
This compound is mainly an auxin analog, which has the properties of a plant growth regulator. It plays a role in regulating hormones in plant growth and development. In addition, it has a broad spectrum of fungicidal activity and can be used as a fungicide in agriculture.
The acid preparation method can be carried out through the following steps:
1. Preparation of N-animal oleoyl indole by condensation of Wuskeimide and animal oleic acid;
2. N-oleoyl indole reacts with acetic anhydride to produce N-oleoyl indole acetate;
3. N-oleoyl indole acetate reacts with silver oxide to give N-oleoyl indole carboxaldehyde;
4. N-animal oleoyl indole carboxaldehyde reacts with methanol to generate chromium acid.
Regarding safety information, acid has no obvious danger under normal use conditions. However, as a chemical, appropriate laboratory safety practices should be followed, including wearing appropriate protective equipment, avoiding inhalation, skin contact and eye contact, and avoiding contact with combustibles and oxidants. In case of accidental contact or accidental ingestion, please seek medical advice immediately.
Last Update：2024-04-10 22:29:15
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