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433-05-6

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433-05-6 Usage

General Description

4-Fluoro-N-propylbenzenesulfonamide is a chemical compound with the molecular formula C9H12FNO2S. It is a derivative of sulfonamide and is commonly used as a building block for the synthesis of pharmaceuticals and agrochemicals. 4-Fluoro-N-propylbenzenesulfonamide is known for its potential biological activity and is often used in medicinal chemistry research as a starting material for the development of new therapeutic agents. Its chemical structure consists of a fluoro-substituted benzene ring attached to a propyl group and a sulfonamide moiety, and it is considered to be a valuable intermediate in the synthesis of various organic compounds with potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 433-05-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 433-05:
(5*4)+(4*3)+(3*3)+(2*0)+(1*5)=46
46 % 10 = 6
So 433-05-6 is a valid CAS Registry Number.

433-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-N-propylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-PROPYL 4-FLUOROBENZENESULFONAMIDE

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:433-05-6 SDS

433-05-6Downstream Products

433-05-6Relevant articles and documents

Discovery of Sulfonamide-Derived Agonists of SOS1-Mediated Nucleotide Exchange on RAS Using Fragment-Based Methods

Sarkar, Dhruba,Olejniczak, Edward T.,Phan, Jason,Coker, Jesse A.,Sai, Jiqing,Arnold, Allison,Beesetty, Yugandhar,Waterson, Alex G.,Fesik, Stephen W.

, p. 8325 - 8337 (2020/09/21)

The nucleotide exchange factor Son of Sevenless (SOS) catalyzes the activation of RAS by converting it from its inactive GDP-bound state to its active GTP-bound state. Recently, we have reported the discovery of small-molecule allosteric activators of SOS1 that can increase the amount of RAS-GTP in cells. The compounds can inhibit ERK phosphorylation at higher concentrations by engaging a feedback mechanism. To further study this process, we sought different chemical matter from an NMR-based fragment screen using selective methyl labeling. To aid this process, several Ile methyl groups located in different binding sites of the protein were assigned and used to categorize the NMR hits into different classes. Hit to lead optimization using an iterative structure-based design paradigm resulted in compounds with improvements in binding affinity. These improved molecules of a different chemical class increase SOS1cat-mediated nucleotide exchange on RAS and display cellular action consistent with our prior results.

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