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Selenocyanic acid, (4-bromophenyl)methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57239-52-8

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57239-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57239-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,3 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57239-52:
(7*5)+(6*7)+(5*2)+(4*3)+(3*9)+(2*5)+(1*2)=138
138 % 10 = 8
So 57239-52-8 is a valid CAS Registry Number.

57239-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromobenzylselenocyanate

1.2 Other means of identification

Product number -
Other names 4-Brombenzylselenocyanat

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:57239-52-8 SDS

57239-52-8Relevant academic research and scientific papers

Synthesis of Monofluoromethyl Selenoethers of Aryl and Alkyl from Organoselenocyanate via One-Pot Reaction

Cao, Yuan,Jiang, Lvqi,Yi, Wenbin

supporting information, p. 4360 - 4368 (2019/08/01)

The first practical and feasible approach for the monofluoromethylselenolation of aryl and alkyl halides via one-pot multistep synthesis using KSeCN and ICFH2 is described. Good yields and broad functional group compatibility were obtained. The successful preparation of monofluoromethylselenolated drug-like compounds good practicability of this method. This protocol offered a number of new monofluoromethyl selenoethers, which would accelerate the use of such compounds in the areas of life science. (Figure presented.).

Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteria

Nasim, Muhammad Jawad,Witek, Karolina,Kincses, Annamária,Abdin, Ahmad Yaman,?es?awska, Ewa,Mar?, Ma?gorzata Anna,Gajdács, Márió,Spengler, Gabriella,Nitek, Wojciech,Latacz, Gniewomir,Karczewska, El?bieta,Kie?-Kononowicz, Katarzyna,Handzlik, Jadwiga,Jacob, Claus

supporting information, p. 6021 - 6031 (2019/04/16)

Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS),

Selenocyanates and diselenides: A new class of potent antileishmanial agents

Plano, Daniel,Baquedano, Ylenia,Moreno-Mateos, David,Font, María,Jiménez-Ruiz, Antonio,Palop, Juan Antonio,Sanmartín, Carmen

experimental part, p. 3315 - 3323 (2011/08/03)

Thirty five selenocyanate and diselenide compounds were subjected to in vitro screening against Leishmania infantum promastigotes and the most active ones were also tested in an axenic amastigote model. In order to establish the selectivity indexes (SI) t

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