5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE
5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE
CAS: 6260-86-2
Molecular Formula: C11H11NO2
5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE - Names and Identifiers
5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE - Physico-chemical Properties
| Molecular Formula | C11H11NO2 |
| Molar Mass | 189.21 |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Class | IRRITANT |
5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE - Upstream Downstream Industry
| Downstream Products | 3-CYANO-5-METHOXY-2-METHYLINDOLE |
5-METHOXY-2-METHYL-1H-INDOLE-3-CARBALDEHYDE - Introduction
It is an organic compound with the chemical formula C11H11NO2.
Nature:
-Appearance: White to light yellow solid;
-Melting point: about 95-97 ° C;
-Solubility: Soluble in organic solvents such as ethanol, dimethyl sulfoxide, etc.
Use:
-is used as a synthetic intermediate in the pharmaceutical field;
-It can also be used as a cosmetic and fragrance additive.
Method:
It can be synthesized by the following steps:
1.5-methoxy-LH-indole -3-carbaldehyde was obtained by substitution reaction under acidic conditions with Urotropine as raw material.
2. Through the methylation reaction, add methylating agents (such as sodium carbonate and methyl iodide) under alkaline conditions to obtain.
Safety Information:
-may have irritating effects on eyes, respiratory system and skin, and attention should be paid to protective measures when touching;
-Avoid contact with oxidants and strong acids during use or storage.
Nature:
-Appearance: White to light yellow solid;
-Melting point: about 95-97 ° C;
-Solubility: Soluble in organic solvents such as ethanol, dimethyl sulfoxide, etc.
Use:
-is used as a synthetic intermediate in the pharmaceutical field;
-It can also be used as a cosmetic and fragrance additive.
Method:
It can be synthesized by the following steps:
1.5-methoxy-LH-indole -3-carbaldehyde was obtained by substitution reaction under acidic conditions with Urotropine as raw material.
2. Through the methylation reaction, add methylating agents (such as sodium carbonate and methyl iodide) under alkaline conditions to obtain.
Safety Information:
-may have irritating effects on eyes, respiratory system and skin, and attention should be paid to protective measures when touching;
-Avoid contact with oxidants and strong acids during use or storage.
Last Update：2024-04-09 02:00:50
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Product Name: 5-Methoxy-2-methylindole-3-carboxaldehyde Visit Supplier Webpage Request for quotation
CAS: 6260-86-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 6260-86-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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