2,3-Dimethyl-3-benzyl-1H-benzo[e]indole

2,3-Dimethyl-3-benzyl-1H-benzo[e]indole - Names and Identifiers

Name	1,2-Dimethyl-1-(phenylmethyl)-1H-benz[e]indole
Synonyms	1,2-Dimethyl-1-(Phenylmethyl)- 1-benzyl-1,2-dimethylbenzo[e]indole 1-benzyl-1,2-dimethyl-1H-benzo[e]indole 1-Benzyl-1,2-dimethyl-1H-benzo[e]indole 2,3-Dimethyl-3-benzyl-1H-benzo[e]indole 1,2-dimethyl-1-(phenylmethyl)-1H-Benz[e]indole 1,2-Dimethyl-1-(phenylmethyl)-1H-benz[e]indole 1,2-Dimethyl-1-(phenylmethyl)-1h-benz[e]indole in stock Factory
CAS	891503-75-6
EINECS	1592732-453-0
InChI	InChI=1/C21H19N/c1-15-21(2,14-16-8-4-3-5-9-16)20-18-11-7-6-10-17(18)12-13-19(20)22-15/h3-13H,14H2,1-2H3

2,3-Dimethyl-3-benzyl-1H-benzo[e]indole - Physico-chemical Properties

Molecular Formula	C21H19N
Molar Mass	285.38
Storage Condition	2-8°C
Refractive Index	1.614

2,3-Dimethyl-3-benzyl-1H-benzo[e]indole - Introduction

1,2-Dimethyl-1-(phenylmethyl)-1H-benz[e]indole is an organic compound with a chemical formula of C21H19N and a relative molecular mass of 281.38. It is a white crystal or solid that decomposes when heated. The main properties and uses of the compound are as follows:

Nature:
-Appearance: White crystal or solid
-Solubility: Good solubility, soluble in organic solvents such as ethanol, dichloromethane and dimethyl sulfoxide
-Melting point: about 160-164 degrees Celsius

Use:
-Fluorescent dye: Due to its good luminescence properties, 1,2-Dimethyl-1-(phenylmethyl)-1H-benz[e]indole can be used as a fluorescent dye, which is widely used in organic light-emitting diodes (OLED), solar cells and other devices.
-Chemical synthesis intermediate: 1,2-Dimethyl-1-(phenylmethyl)-1H-benz[e]indole can also be used as a chemical synthesis intermediate for the synthesis of other organic compounds.

Preparation Method:
1,2-Dimethyl-1-(phenylmethyl)-1H-benz[e]indole can be prepared by a variety of methods. The commonly used methods are:
1. Under alkaline conditions, benzo [e] indole reacts with methylbenzyl alcohol to introduce methyl groups through nucleophilic substitution reaction.
2. Use methyl magnesium chloride and benzonitrile to react, and then obtain the target product through cyclization reaction.

Safety Information:
Toxicity and safety information for this compound has not been clearly reported. However, because it is a chemical, general laboratory safety procedures should be followed when using or handling it, such as wearing appropriate protective equipment, avoiding contact with skin or inhalation of its dust, and proper storage and disposal of waste. Attention should be paid to good ventilation and safety control measures during use.

Last Update：2024-04-10 22:29:15