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2-((2-selenocyanatoethyl)carbamoyl)phenyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1850293-95-6

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1850293-95-6 Usage

Chemical structure

The compound consists of a phenyl acetate group and a selenocyanatoethylcarbamoyl group.

Usage

It is commonly used in organic synthesis and pharmaceutical research.

Pharmacological activities

The compound has potential pharmacological activities, including anti-inflammatory and antimicrobial properties.

Selenocyanatoethylcarbamoyl group

This group has been studied for its potential antioxidant and anti-cancer properties.

Biological and medical applications

2-((2-selenocyanatoethyl)carbamoyl)phenyl acetate has shown promise in various biological and medical applications.

Ongoing research

The compound continues to be a subject of research in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1850293-95-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,5,0,2,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1850293-95:
(9*1)+(8*8)+(7*5)+(6*0)+(5*2)+(4*9)+(3*3)+(2*9)+(1*5)=186
186 % 10 = 6
So 1850293-95-6 is a valid CAS Registry Number.

1850293-95-6Upstream product

1850293-95-6Downstream Products

1850293-95-6Relevant academic research and scientific papers

Design, Synthesis, and Biological Evaluation of Novel Selenium (Se-NSAID) Molecules as Anticancer Agents

Plano, Daniel,Karelia, Deepkamal N.,Pandey, Manoj K.,Spallholz, Julian E.,Amin, Shantu,Sharma, Arun K.

, p. 1946 - 1959 (2016)

The synthesis and anticancer evaluation of novel selenium-nonsteroidal anti-inflammatory drug (Se-NSAID) hybrid molecules are reported. The Se-aspirin analogue 8 was identified as the most effective agent in reducing the viability of different cancer cell

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