2,5,6-Trichloro-1H-benzo[d]imidazole

2,5,6-Trichloro-1H-benzo[d]imidazole - Names and Identifiers

Name	2,5,6-TRICHLORO-1H-BENZIMIDAZOLE
Synonyms	2,5,6-Trichlorobenzimidazole Benzimidazole, 2,5,6-trichloro- 2,5,6-TRICHLORO-1H-BENZIMIDAZOLE 2,5,6-trichloro-3aH-benzimidazole 1H-Benzimidazole, 2,5,6-trichloro- 2,5,6-trichloro-1H-1,3-benzodiazole 2,5,6-Trichloro-1H-benzo[d]imidazole 2,5,6-trichloro-1H-benzo[d]imidazole
CAS	16865-11-5

2,5,6-Trichloro-1H-benzo[d]imidazole - Physico-chemical Properties

Molecular Formula	C7H3Cl3N2
Molar Mass	221.47
Density	1.691±0.06 g/cm3(Predicted)
Boling Point	399.3±45.0 °C(Predicted)
pKa	6.87±0.10(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Use	This product is for scientific research only and shall not be used for other purposes.

2,5,6-Trichloro-1H-benzo[d]imidazole - Introduction

2,5, is an organic compound having the following properties:

1. Appearance: 2,5, is a colorless crystalline solid.

2. Solubility: It is almost insoluble in water, but soluble in organic solvents such as ethanol, ether, etc.

3. Stability: 2,5, is relatively stable at room temperature, but may decompose at high temperature or in the presence of strong acids and alkalis.

4. Chemical reaction: it is an alkaline substance, can react with acid to generate salt. It can also participate in some important chemical reactions, such as nucleophilic substitution reaction, addition reaction and so on.
The main uses of
2,5, will include:

1. Advanced photosensitive material: Due to its structural characteristics, it can be used to prepare photosensitive materials, such as photosensitive film, photoresist, etc., and is widely used in printing, electronics and optical industries.

2. Pharmaceutical field: 2,5, Ni has certain antibacterial and antiviral activity, and can be used to synthesize intermediates for Antibacterial Drugs and antiviral drugs.

The methods for preparing 2,5, Ni are mainly as follows:

1. Chlorobenzene substitution method: An appropriate amount of 2,5, 6-trichlorobenzene is reacted with imidazole in an acidic solution, and 2,5, benzol is synthesized by substitution reaction.

2. Electrophilic substitution method: 2,5, Ni can be used to carry out nucleophilic substitution reaction on the electrophilic reagent, and the target compound can be synthesized by introducing different substituents.

The following safety information is required when using and handling 2,5, 0.5:

1. Operation should wear personal protective equipment, such as experimental gloves, eye protection glasses.

2. Avoid inhalation of gas or dust, avoid contact with skin or eyes.

3. Use in a well-ventilated place and avoid contact with harmful substances such as oxidants, strong acids, and strong alkalis.

4. Storage should be sealed and stored in a shading, dry and ventilated environment.

Last Update：2024-04-09 21:21:28