2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl-

2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl- - Names and Identifiers

Name	2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl-
Synonyms	2-Mecapto-1-methylbenzimidazole 1-Methyl-1H-Benzimidazole-2-Thio 2-Mercapto-1-Methylbenzo[d]iMidazole 1-METHYL-1H-BENZIMIDAZOLE-2-THIOL 95 1-Methyl-1H-benzo[d]iMidazole-2-thiol 1,3-Dihydro-1-Methyl-2H-benziMidazole-2-thione 2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl- 2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl-(9CI)
CAS	2360-22-7

2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl- - Physico-chemical Properties

Molecular Formula	C8H8N2S
Molar Mass	164.23
Density	1.33 g/cm³
Melting Point	193-197 °C (lit.)
Boling Point	268.7 °C at 760 mmHg
Flash Point	116.3 °C
Storage Condition	Room Temprature

2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl- - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.
WGK Germany	3
Hazard Class	IRRITANT

2H-Benzimidazole-2-thione,1,3-dihydro-1-methyl- - Introduction

1,3-dihydro-1-methyl-, also known as 1,3-dihydro-1-methyl-, is an organic compound.

The properties of the compound are as follows:
1. Molecular formula: C9H8N2S
2. Molecular Weight: 180.24g/mol
3. Appearance: colorless or light yellow solid
4. Melting Point: 128-131 ° C
5. Boiling point: 337 ° C

The main uses of this compound are as follows:
1. Used as an intermediate in organic synthesis and can be used to synthesize other organic compounds.
2. In the field of medicine, it can be used as the starting material of drug synthesis.
3. Can be used as antibacterial agents, pesticides and other pesticides raw materials.
4. In the dye and coating industry, it can be used for dye synthesis and pigment preparation.

There are many ways to make Ti, 1,3-dihydro-1-methyl-, one of which is commonly used as follows:
Through the reaction of the amino group of benzimidazole and thioacetyl chloride, a nucleophilic addition reaction occurs under the catalysis of a base to generate the product, 1,3-dihydro-1-methyl-.

Safety information and precautions regarding this compound:
1., 1,3-dihydro-1-methyl-has certain irritation and toxicity, please wear personal protective equipment, such as chemical protective gloves, glasses, etc.
2. During operation, attention should be paid to prevent contact with skin, eyes or respiratory system to avoid injury or allergic reaction.
3. During storage and transportation, place 1,3-dihydro-1-methyl-in a dry, well-ventilated place away from fire and oxidizing agents.
4. When using or handling the compound, the corresponding laboratory safety procedures and regulations should be followed.

Last Update：2024-04-09 21:54:55