Welcome to LookChem.com Sign In|Join Free

CAS

  • or

593960-71-5

Post Buying Request

593960-71-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

593960-71-5 Usage

Description

2-chloro-5-(2-oxopropyl)benzene-1-sulfonyl chloride is a chemical compound with the molecular formula C10H10ClO3S. It is a sulfonyl chloride derivative and a reactive intermediate in the synthesis of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
2-chloro-5-(2-oxopropyl)benzene-1-sulfonyl chloride is used as a reactive intermediate for the synthesis of various sulfonyl-containing compounds which are utilized as pharmaceuticals. Its reactivity allows for the creation of a wide range of drug molecules.
Used in Agrochemical Industry:
2-chloro-5-(2-oxopropyl)benzene-1-sulfonyl chloride is used as a reactive intermediate for the synthesis of sulfonyl-containing compounds utilized as agrochemicals. Its ability to form various chemical structures makes it valuable in developing effective agricultural products.
Used in Dye Industry:
2-chloro-5-(2-oxopropyl)benzene-1-sulfonyl chloride is used as a reactive intermediate in the production of dyes. The sulfonyl chloride group allows for the attachment of various functional groups, creating a diverse range of dyes with different properties.
It is a highly reactive compound that is handled with caution in laboratory settings due to its ability to react violently with water and other reactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 593960-71-5 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, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 593960-71:
(8*5)+(7*9)+(6*3)+(5*9)+(4*6)+(3*0)+(2*7)+(1*1)=205
205 % 10 = 5
So 593960-71-5 is a valid CAS Registry Number.

593960-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-5-(2-oxopropyl)benzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 2-chloro-5-(2-oxo-propyl)-benzenesulfonyl chloride

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:593960-71-5 SDS

593960-71-5Relevant articles and documents

Design and Structural Characterization of Potent and Selective Inhibitors of Phosphatidylinositol 4 Kinase IIIβ

Rutaganira, Florentine U.,Fowler, Melissa L.,McPhail, Jacob A.,Gelman, Michael A.,Nguyen, Khanh,Xiong, Anming,Dornan, Gillian L.,Tavshanjian, Brandon,Glenn, Jeffrey S.,Shokat, Kevan M.,Burke, John E.

, p. 1830 - 1839 (2016/03/22)

Type III phosphatidylinositol 4-kinase (PI4KIIIβ) is an essential enzyme in mediating membrane trafficking and is implicated in a variety of pathogenic processes. It is a key host factor mediating replication of RNA viruses. The design of potent and specific inhibitors of this enzyme will be essential to define its cellular roles and may lead to novel antiviral therapeutics. We previously reported the PI4K inhibitor PIK93, and this compound has defined key functions of PI4KIIIβ. However, this compound showed high cross reactivity with class I and III PI3Ks. Using structure-based drug design, we have designed novel potent and selective (>1000-fold over class I and class III PI3Ks) PI4KIIIβ inhibitors. These compounds showed antiviral activity against hepatitis C virus. The co-crystal structure of PI4KIIIβ bound to one of the most potent compounds reveals the molecular basis of specificity. This work will be vital in the design of novel PI4KIIIβ inhibitors, which may play significant roles as antiviral therapeutics.

THIAZOLE DERIVATIVES AS INHIBITORS OF P13 KINASE

-

Page/Page column 34, (2008/06/13)

Compounds of formula (I) are inhibitors of P13 kinase activity, and useful in treatment of, inter alia, autoimmune, inflammatory and proliferative diseases: wherein: s is 0 or 1; U is hydrogen or halogen; X is -(C=O), an optionally substituted divalent ph

5-PHENYLTHIAZOLE DERIVATIVES AND THEIR USE AS PI3 KINASE INHIBITORS

-

Page 37, (2010/02/08)

-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 593960-71-5