1-propyl-3-indolecarboxaldehyde
1-Propyl-1H-indole-3-carbaldehyde
CAS: 119491-08-6
Molecular Formula: C12H13NO
1-propyl-3-indolecarboxaldehyde - Names and Identifiers
1-propyl-3-indolecarboxaldehyde - Physico-chemical Properties
| Molecular Formula | C12H13NO |
| Molar Mass | 187.24 |
| Density | 1.06±0.1 g/cm3(Predicted) |
| Melting Point | 65-66.5 °C |
| Boling Point | 339.8±15.0 °C(Predicted) |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD03905843 |
1-propyl-3-indolecarboxaldehyde - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Class | IRRITANT |
1-propyl-3-indolecarboxaldehyde - Introduction
The formula is C13H13NO, which is an organic compound with a molecular weight of 203.25g/mol.
The compound is a liquid with a smoke smell and has a yellow to brown appearance. It has good solubility and is readily soluble in solvents such as ethanol, ether and chloroform.
It is often used as an intermediate in chemical synthesis. It can be used to synthesize various organic compounds, such as drugs, fragrances and dyes. Its aroma has led to its widespread use in the flavor and fragrance industry for the formulation of a variety of perfumes, aromatherapy and personal care products.
Preparation can be done in a variety of ways. One common approach is to synthesize by a route through a multi-step reaction, starting with Indole. Specifically, the acylated product can be obtained by acylating Indole first, and then reducing it under appropriate conditions.
The compound is a liquid with a smoke smell and has a yellow to brown appearance. It has good solubility and is readily soluble in solvents such as ethanol, ether and chloroform.
It is often used as an intermediate in chemical synthesis. It can be used to synthesize various organic compounds, such as drugs, fragrances and dyes. Its aroma has led to its widespread use in the flavor and fragrance industry for the formulation of a variety of perfumes, aromatherapy and personal care products.
Preparation can be done in a variety of ways. One common approach is to synthesize by a route through a multi-step reaction, starting with Indole. Specifically, the acylated product can be obtained by acylating Indole first, and then reducing it under appropriate conditions.
Last Update：2024-04-09 02:00:56
