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19559-59-2

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19559-59-2 Usage

General Description

Potassium dichloroacetate is a chemical compound that is derived from dichloroacetic acid and contains the elements potassium, chlorine, carbon, and hydrogen. It is known for its potential antitumor and anticancer properties, as it has been studied for its ability to inhibit the proliferation of cancer cells and induce apoptosis. Additionally, it has been investigated for its potential to upregulate the mitochondrial function and promote the regulation of glucose metabolism, which may contribute to its anti-cancer effects. Potassium dichloroacetate has also been researched for its potential role in regulating the activity of the pyruvate dehydrogenase complex, which is involved in the metabolism of glucose. Overall, potassium dichloroacetate shows promise as a potential therapeutic agent for cancer treatment, although further research is needed to fully understand its mechanisms of action and potential clinical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19559-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19559-59:
(7*1)+(6*9)+(5*5)+(4*5)+(3*9)+(2*5)+(1*9)=152
152 % 10 = 2
So 19559-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H2Cl2O2.K/c3-1(4)2(5)6;/h1H,(H,5,6);/q;+1/p-1

19559-59-2 Well-known Company Product Price

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  • Aldrich

  • (348082)  Potassiumdichloroacetate  98%

  • 19559-59-2

  • 348082-10G

  • 493.74CNY

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19559-59-2SDS

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 potassium,2,2-dichloroacetate

1.2 Other means of identification

Product number -
Other names Dichlor-essigsaeure,Kalium-Verbindung

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:19559-59-2 SDS

19559-59-2Relevant articles and documents

Iminophenylthiazolidines, process of preparation and method of use

-

, (2008/06/13)

A 2-iminophenyl thiazolidine having the formula STR1 wherein R is hydrogen or methyl; R1 is halo, nitro, cyano, C1 -C4 alkyl, C1 -C4 alkoxy, perhalomethyl, difluoromethyl, pentafluoroethyl, trifluoromethylthhio, difluoromethoxy, trifluoromethoxy, tetrafluoroethoxy, methylsulfonyl, C1 -C4 alkyloxyiminomethyl, benzyloxyiminomethyl, 1-(C1 -C4 alkyl)-oxyiminoethyl or 1-benzyloxyiminoethyl; R2 is hydrogen or halo; R3 and R4 are independently hydrogen, halo, nitro, cyano, C1 -C4 haloalkyl, C1 -C4 alkyl, C1 -C4 fluoroalkoxy, C1 -C4 alkoxy or C1 -C4 alkylthio; and X is hydrogen or halogen. Also disclosed is a process for making the compounds and a method of use which comprises applying the compound or composition to the locus where control is desired.

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