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(R)-2-Chloro-2-oxo-1-phenylethyl dichloroacetate, a chiral dichloroacetate derivative with the molecular formula C10H8Cl4O3, is a compound featuring a phenyl group and two chlorine atoms. This molecule is known for its potential inhibitory effects on cancer cell proliferation through the activation of mitochondrial metabolism, making it a promising candidate for pharmaceutical applications.

40512-60-5

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40512-60-5 Usage

Uses

Used in Pharmaceutical Industry:
(R)-2-Chloro-2-oxo-1-phenylethyl dichloroacetate is used as a potential anti-cancer agent for its ability to inhibit cancer cell proliferation by activating mitochondrial metabolism. (R)-2-Chloro-2-oxo-1-phenylethyl dichloroacetate holds promise in the development of novel cancer treatments, particularly for solid malignancies.
Additionally, it is used as a potential treatment for metabolic disorders due to its impact on mitochondrial metabolism, offering a new avenue for therapeutic intervention in conditions related to metabolic dysfunction.
Used in Chemical Research and Development:
Owing to its unique structure and properties, (R)-2-Chloro-2-oxo-1-phenylethyl dichloroacetate may also find applications in various chemical research and development fields. Its potential uses could include the synthesis of new compounds, the study of its interactions with biological systems, and the exploration of its properties for industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 40512-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,1 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40512-60:
(7*4)+(6*0)+(5*5)+(4*1)+(3*2)+(2*6)+(1*0)=75
75 % 10 = 5
So 40512-60-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H7Cl3O3/c11-8(12)10(15)16-7(9(13)14)6-4-2-1-3-5-6/h1-5,7-8H/t7-/m1/s1

40512-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name R-O-dichloroacetylmandeloyl chloride

1.2 Other means of identification

Product number -
Other names Dichloracetylmandeloylchlorid

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:40512-60-5 SDS

40512-60-5Upstream product

40512-60-5Relevant academic research and scientific papers

Semisynthetic cephalosporins. Synthesis and structure activity relationships of 7 mandelamido 3 cephem 4 carboxylic acids

Hoover,Dunn,Jakas,Lam,Taggart,Guarini,Phillips

, p. 34 - 41 (2007/10/06)

The synthesis, microbiological profile, and in vivo effectiveness in laboratory animals of a broad spectrum cephalosporin, 7(R) mandelamidocephalosporanic acid (1), are described. A number of derivatives and analogs of 1 were prepared and their structure activity relationships are discussed.

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