TIMTEC-BB SBB007573
7-Ethylindole
CAS: 22867-74-9
Molecular Formula: C10H11N
TIMTEC-BB SBB007573 - Names and Identifiers
| Name | 7-Ethylindole |
| Synonyms | 7-ETHYLINDOLE 7-ETHYL-INDOL 7-Ethylindole 7-Ethyl-1H-indole 7-ETHYLCAMPTOTHECIN 1H-indole, 7-ethyl- TIMTEC-BB SBB007573 7-ETHYLINDOLE(ETODOLAC INTERMEDIATE) |
| CAS | 22867-74-9 |
| EINECS | 682-584-2 |
| InChI | InChI=1/C10H11N/c1-2-8-4-3-5-9-6-7-11-10(8)9/h3-7,11H,2H2,1H3 |
TIMTEC-BB SBB007573 - Physico-chemical Properties
| Molecular Formula | C10H11N |
| Molar Mass | 145.2 |
| Density | 1.058g/mLat 20°C(lit.) |
| Melting Point | 82.5°C (estimate) |
| Boling Point | 230 °C |
| Flash Point | 230°C |
| Water Solubility | INSOLUBLE |
| Solubility | Chloroform (Slightly), Methanol (Slightly) |
| Vapor Presure | 0.00592mmHg at 25°C |
| Appearance | Oil |
| Specific Gravity | 1.058 |
| Color | Clear Colorless to Light Brown |
| BRN | 1238356 |
| pKa | 17.30±0.30(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | n20/D 1.603 |
| Physical and Chemical Properties | Light yellow transparent liquid. |
TIMTEC-BB SBB007573 - Risk and Safety
| Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29339980 |
TIMTEC-BB SBB007573 - Introduction
7-Ethylindole is an organic compound with the chemical formula C10H11N. It is a derivative of indole with specific physical and chemical properties.
Nature:
-Appearance: 7-Ethylindole is white to light yellow solid.
-Solubility: It is soluble in ethanol, chloroform and dichloromethane and other organic solvents, insoluble in water.
-Melting point: Its melting point is usually between 50-60 degrees Celsius.
-Odor: It has a special aromatic smell.
Use:
7-Ethylindole has certain application value in the field of organic synthesis and medicine. Some of the main uses include:
-As a raw material in Organic Synthesis: Due to the presence of indole rings and ethyl groups in its structure, 7-Ethylindole can be used as a starting material in organic synthesis for the preparation of various indole compounds.
-Research in the field of medicine: 7-Ethylindole and its derivatives are widely used in the field of anti-virus, anti-tumor and anti-inflammatory research.
Method:
There are many preparation methods for 7-Ethylindole. The following is one of the common preparation methods:
1. The two chemicals 4-nitro-2-ethylphenol and 1,2-cyclohexanedione react to produce 2-ethyl-1-[4-(Nitro) phenoxy] Cyclohexyl -1-one.
2. The compound obtained in the previous step is subjected to reduction treatment to obtain 2-ethyl -1-[4-aminophenoxy] cyclo -1-one.
3. Under the action of high temperature and catalyst, the compound obtained in the previous reaction is reacted with ammonia to generate 7-Ethylindole.
Safety Information:
For the safe handling of chemicals, the following are some common safety information:
- 7-Ethylindole is a chemical that requires protective gloves, goggles and protective clothing when used.
-During operation, pay attention to avoid inhalation or contact with skin.
-Store away from fire and flammable materials.
-If skin or eye contact occurs, rinse immediately with plenty of water and seek medical help.
-Adhere to local regulations and rules for proper disposal of residual chemicals and waste.
Nature:
-Appearance: 7-Ethylindole is white to light yellow solid.
-Solubility: It is soluble in ethanol, chloroform and dichloromethane and other organic solvents, insoluble in water.
-Melting point: Its melting point is usually between 50-60 degrees Celsius.
-Odor: It has a special aromatic smell.
Use:
7-Ethylindole has certain application value in the field of organic synthesis and medicine. Some of the main uses include:
-As a raw material in Organic Synthesis: Due to the presence of indole rings and ethyl groups in its structure, 7-Ethylindole can be used as a starting material in organic synthesis for the preparation of various indole compounds.
-Research in the field of medicine: 7-Ethylindole and its derivatives are widely used in the field of anti-virus, anti-tumor and anti-inflammatory research.
Method:
There are many preparation methods for 7-Ethylindole. The following is one of the common preparation methods:
1. The two chemicals 4-nitro-2-ethylphenol and 1,2-cyclohexanedione react to produce 2-ethyl-1-[4-(Nitro) phenoxy] Cyclohexyl -1-one.
2. The compound obtained in the previous step is subjected to reduction treatment to obtain 2-ethyl -1-[4-aminophenoxy] cyclo -1-one.
3. Under the action of high temperature and catalyst, the compound obtained in the previous reaction is reacted with ammonia to generate 7-Ethylindole.
Safety Information:
For the safe handling of chemicals, the following are some common safety information:
- 7-Ethylindole is a chemical that requires protective gloves, goggles and protective clothing when used.
-During operation, pay attention to avoid inhalation or contact with skin.
-Store away from fire and flammable materials.
-If skin or eye contact occurs, rinse immediately with plenty of water and seek medical help.
-Adhere to local regulations and rules for proper disposal of residual chemicals and waste.
Last Update：2024-04-09 21:04:16
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Spot supply
Product Name: 7-Ethylindole Request for quotationCAS: 22867-74-9
Tel: +86-17551318830
Email: r@reformchem.com
Mobile: +86-17551318830
QQ: 3785839865
Product Name: 7-Ethylindole Request for quotation
CAS: 22867-74-9
Tel: 17505222756
Email: pules.cn@gmail.com
Mobile: +86-17551318830
Wechat: 17505222756
CAS: 22867-74-9
Tel: 17505222756
Email: pules.cn@gmail.com
Mobile: +86-17551318830
Wechat: 17505222756
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