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Benzenesulfonamide, 5-(1-bromo-2-oxopropyl)-2-methoxy-, is a chemical compound with the molecular formula C10H10BrNO3S. It is a derivative of benzenesulfonamide, featuring a 1-bromo-2-oxopropyl group at the 5-position and a methoxy group at the 2-position. Benzenesulfonamide, 5-(1-bromo-2-oxopropyl)-2-methoxy- is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly in the development of drugs targeting various therapeutic areas. Its unique structure allows for further functionalization and modification, making it a valuable intermediate in organic synthesis.

593960-46-4

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593960-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 593960-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,3,9,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 593960-46:
(8*5)+(7*9)+(6*3)+(5*9)+(4*6)+(3*0)+(2*4)+(1*6)=204
204 % 10 = 4
So 593960-46-4 is a valid CAS Registry Number.

593960-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(1-bromo-2-oxopropyl)-2-methoxybenzenesulfonamide

1.2 Other means of identification

Product number -
Other names Benzenesulfonamide,5-(1-bromo-2-oxopropyl)-2-methoxy

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:593960-46-4 SDS

593960-46-4Downstream Products

593960-46-4Relevant academic research and scientific papers

2-Alkyloxazoles as potent and selective PI4KIIIβ inhibitors demonstrating inhibition of HCV replication

Keaney, Erin P.,Connolly, Michael,Dobler, Markus,Karki, Rajeshri,Honda, Ayako,Sokup, Samantha,Karur, Subramanian,Britt, Shawn,Patnaik, Anup,Raman, Prakash,Hamann, Lawrence G.,Wiedmann, Brigitte,Lamarche, Matthew J.

, p. 3714 - 3718 (2014/09/17)

Synthesis and SAR of 2-alkyloxazoles as class III phosphatidylinositol-4- kinase beta (PI4KIIIβ) inhibitors is described. These compounds demonstrate that inhibition of PI4KIIIβ leads to potent inhibition of HCV replication as observed in genotype (GT) 1a and 1b replicon and GT2a JFH1 virus assays in vitro.

5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS

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Page/Page column 45, (2010/02/07)

Compounds of Formula I in free or salt form, wherein R1,R2,R3,R4, and R5, have the meanings as indicated in the specification, are useful for treating diseases mediated by phosphatidylinositol 3-kinase. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.

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