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848649-94-5

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848649-94-5 Usage

Description

6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE is a chemical compound with the molecular formula C8H6BrNS. It is a derivative of indole that contains a bromine and a sulfur atom. 6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE is commonly used in organic synthesis and pharmaceutical research as a building block for creating various bioactive molecules. It has been studied for potential pharmacological properties, such as anti-cancer, anti-inflammatory, and antimicrobial activities. Additionally, 6-Bromo-1,3-dihydro-indole-2-thione has shown potential in the development of new drugs and therapeutic agents.

Uses

Used in Pharmaceutical Research:
6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE is used as a building block for creating various bioactive molecules for pharmaceutical research. Its unique structure allows for the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE is used as a key intermediate in organic synthesis, enabling the creation of a wide range of chemical compounds with potential applications in various industries.
Used in Anticancer Applications:
6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE is studied for its potential anti-cancer properties, making it a candidate for the development of new cancer treatments.
Used in Anti-inflammatory Applications:
6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE is researched for its potential anti-inflammatory activities, which could lead to the development of new treatments for inflammatory conditions.
Used in Antimicrobial Applications:
6-BROMO-1,3-DIHYDRO-INDOLE-2-THIONE has shown potential in antimicrobial activities, making it a candidate for the development of new antibiotics and antifungal agents.

Check Digit Verification of cas no

The CAS Registry Mumber 848649-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,6,4 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 848649-94:
(8*8)+(7*4)+(6*8)+(5*6)+(4*4)+(3*9)+(2*9)+(1*4)=235
235 % 10 = 5
So 848649-94-5 is a valid CAS Registry Number.

848649-94-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-1,3-dihydro-2H-indole-2-thione

1.2 Other means of identification

Product number -
Other names 6-bromoindan-1-ylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:848649-94-5 SDS

848649-94-5Downstream Products

848649-94-5Relevant articles and documents

Synthesis of 2-(Arylthio)indolenines via Chemoselective Arylation of Thio-Oxindoles with Arynes

Saputra, Adi,Fan, Rong,Yao, Tuanli,Chen, Jian,Tan, Jiajing

supporting information, p. 2683 - 2688 (2020/05/18)

A chemoselective S-arylation reaction of thio-oxindoles with arynes is presented. The reaction was performed under mild conditions and provided a straightforward synthesis of 2-(arylthio)indolenines in good to excellent yields. Besides, this simple operat

Concise syntheses of the cruciferous phytoalexins brassilexin, sinalexin, wasalexins, and analogues: Expanding the scope of the Vilsmeier formylation

Pedras, M. Soledade C.,Jha, Mukund

, p. 1828 - 1834 (2007/10/03)

(Chemical Equation Presented) Efficient syntheses of the phytoalexins brassilexin, sinalexin, and analogues are demonstrated through the application of the Vilsmeier formylation to indoline-2-thiones followed by a new aqueous ammonia workup procedure. Similarly, a very concise two-pot synthesis of the phytoalexins wasalexins using sequential formylation-amination of indolin-2-ones is described. Remarkably, this novel aqueous ammonia workup allows the sequential one-pot formylation-amination, expanding substantially the scope of the Vilsmeier formylation of both indoline-2-thiones and indolin-2-ones. The examination of the formylation-amination reaction and optimization of conditions, as well as the syntheses and antifungal activities of several brassilexin analogues, are reported.

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