1,1,2-Trimethyl-1H-benz[e]indole CAS 41532-84-7

1. Nature:
TMBI is a white crystalline solid.

Preparation:
The preparation of TMBI is generally achieved by chemical synthesis. A common method is to add 1,1' -dimethyl-4,4' -dithiourea to 4-bromobenzaldehyde, which reacts to form TMBI with the catalysis of a base. Reaction conditions can be adjusted according to specific requirements.

Safety information:
- TMBI is irritating, avoid contact with skin and eyes. In case of contact, rinse immediately with water.
- TMBI is toxic to the environment and should be avoided from entering water and soil.
- Personal protective measures such as protective gloves, safety glasses and laboratory ventilation should be used during operation.
- TMBI should be kept away from open flames and high temperatures and stored in a cool, dry place.

1,1,2-Trimethyl-1H-benzo[e]indole can be used as an indole pH fluorescent probe and can be used for intracellular pH detection and cell marking. It can also be used as a novel nanocarrier-based near-infrared optical probes for in-vivo tumor imaging.

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Product Name:	1,1,2-Trimethyl-1H-benz[e]indole
Synonyms:	1,1,2-TRIMETHYL-1H-BENZ(E)INDOLE /2,3,3-TRIMETHYL-4.5-BENZO-3H- INDOLE;2,3,3-TRIMETHYL-4,5-BENZOINDOLENINE(2,3,3-TRIMETHYL-BENZOINDOLENINE)(TBA);2,3,3-Trimethylbenzoeüindolenine, 97%;2,3,3-Trimethyl-4,5-benzoindole;1,2-Trimethyl-1H-benz[e]indole ,98%;1,1,2-Trimethyl-1H-benz[e]indole,96%;1,1,2-Trimethylbenzo[e]indolenine;2-TriMethyl-1H-benz[e]indole
CAS:	41532-84-7
MF:	C15H15N
MW:	209.29
EINECS:	255-429-8
Product Categories:	Heterocycle-Indole series;
Mol File:	41532-84-7.mol

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