舍他康唑EP杂质B

舍他康唑EP杂质B - Names and Identifiers

Name	3-(bromomethyl)-7-chloro benzo[b]thiophene
Synonyms	FI 7009 Sertaconazole impurity B Sertaconazole EP Impurity B Sertaconazole Nitrate EP Impurity B 3-(Bromomethyl)-7-chloro-benzothiophene 3-bromomethyl-7-chlorobenzo[b]thiophine 3-(Bromomethyl)-7-chloro-1-benzothiophene 3-(Bromomethyl)-7-chlorobenzo[b]thiophene 3-(bromomethyl)-7-chloro benzo[b]thiophene 3-(BROMOMETHYL)-7-CHLORO BENZO[B]THIOPHENE benzo[b]thiophene, 3-(bromomethyl)-7-chloro- Benzo[b]thiophene, 3-(bromomethyl)-7-chloro-
CAS	17512-61-7
EINECS	1308068-626-2
InChI	InChI=1/C9H6BrClS/c10-4-6-5-12-9-7(6)2-1-3-8(9)11/h1-3,5H,4H2

舍他康唑EP杂质B - Physico-chemical Properties

Molecular Formula	C9H6BrClS
Molar Mass	261.57
Density	1.693±0.06 g/cm3(Predicted)
Boling Point	345.5±27.0 °C(Predicted)
Flash Point	162.8°C
Vapor Presure	0.000122mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.704

舍他康唑EP杂质B - Introduction

3-(bromomethyl)-7-chloro benzo [B] thiophene is an organic compound containing bromine, chlorine and sulfur elements. The following is a description of its nature, use, preparation and safety information:

Nature:
3-(bromomethyl)-7-chlorophyll benzo [B] thiophene is a very stable compound with a light yellow to reddish brown crystalline solid form. It has a low solubility, can be decomposed under high temperature and strong acid conditions, and is more stable to air and light. In chemical reactions, it can occur electrophilic substitution, nucleophilic reactions and cycloaddition reactions.

Use:
3-(bromomethyl)-7-chloro benzo [B] thiophene is commonly used as a starting material or reagent in organic synthesis reactions. It has potential anti-cancer activity in the field of medicine, so it is widely studied for the development of anti-tumor drugs. In addition, it can also be used for dye synthesis, pesticide preparation and organic optoelectronic materials research.

Method:
The synthesis of 3-(bromomethyl)-7-chloro benzo [B] thiophene is usually obtained by reacting benzo [B] thiophene with methyl bromide or stannous chloride. Benzo [B] thiophene is first reacted with methyl bromide or stannous chloride, and then the target product is obtained by oxidation or reduction reaction.

Safety Information:
3-(bromomethyl)-7-chlorophyll benzo [B] thiophene is an organic compound, so you should pay attention to safety during operation. It may cause irritation to the human body, so wear appropriate protective equipment such as gloves and safety glasses when handling. In addition, make sure to operate in a well-ventilated area. If it comes into contact with the skin or inhales into the lungs, wash it immediately or seek medical assistance. Please strictly follow the relevant safety operation procedures.

Last Update：2024-04-09 20:52:54