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209968-27-4

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209968-27-4 Usage

Description

Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]is a chemical compound that belongs to the class of sulfonamide compounds. It contains a benzene ring attached to a sulfonamide group and a 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]chain. Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]has potential biological activity and is used in medicinal chemistry for drug development.

Uses

Used in Medicinal Chemistry:
Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a versatile building block in the development of new drugs with potential therapeutic applications.
Used in Drug Development:
Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]is used as a lead compound in the discovery and optimization of new drugs. Its potential biological activity makes it a promising candidate for further research and development, with the aim of identifying novel therapeutic agents for various diseases and conditions.
Used in Chemical Synthesis:
Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]is used as a reactant in various chemical reactions, enabling the synthesis of a wide range of organic compounds. Its presence in these reactions can lead to the formation of new molecules with diverse properties and potential applications.
Used in Pharmaceutical Production:
Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]may be used in the production of pharmaceuticals, where it can contribute to the development of new drugs or the improvement of existing ones. Its presence in the manufacturing process can enhance the efficacy, safety, or stability of the final product.
Used as a Research Tool:
Benzenesulfonamide, 4-bromo-N-[2-(1-pyrrolidinyl)ethyl]can be used as a research tool in the study of biological processes and the development of novel therapeutic agents. Its unique structure and potential biological activity make it a valuable asset in the exploration of new scientific frontiers and the advancement of medical knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 209968-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,9,6 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 209968-27:
(8*2)+(7*0)+(6*9)+(5*9)+(4*6)+(3*8)+(2*2)+(1*7)=174
174 % 10 = 4
So 209968-27-4 is a valid CAS Registry Number.

209968-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-N-(2-pyrrolidin-1-ylethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names -

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:209968-27-4 SDS

209968-27-4Relevant articles and documents

Substituted halogenated arylsulfonamides: A new class of σ receptor binding tumor imaging agents

John, Christy S.,Lim, Benjamin B.,Vilner, Bertold J.,Geyer, Brian C.,Bowen, Wayne D.

, p. 2445 - 2450 (1998)

The discovery of a series of novel halogenated arylsulfonamides (HAS) as new σ receptor binding tumor imaging agents is described. Several substituted halogenated sulfonamides have been prepared and characterized. Target compounds were examined for their

PYRIMIDINE COMPOUNDS AND METHODS OF USE

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Page/Page column 41, (2010/11/24)

The invention provides pyrimidine compounds having formula (A): The pyrimidine compounds of the invention are capable of inhibiting kinases, such as members of the Src kinase family, and various other specific receptor and non-receptor kinases.

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