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22541-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22541-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,4 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22541-48:
(7*2)+(6*2)+(5*5)+(4*4)+(3*1)+(2*4)+(1*8)=86
86 % 10 = 6
So 22541-48-6 is a valid CAS Registry Number.

22541-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name selenide

1.2 Other means of identification

Product number -
Other names SE-2

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:22541-48-6 SDS

22541-48-6Downstream Products

22541-48-6Related news

Synthesis and characterization of nickel doped zinc SELENIDE (cas 22541-48-6) nanospheres for nonlinear optical applications07/16/2019

Phase purity plays an important role in determining the properties of the material and its subsequent applications which depends on the synthesis conditions and dopant concentrations. Phase pure zinc selenide and nickel doped zinc selenide nanoparticles were synthesized by hydrothermal method us...detailed

Fabrication of IR windows grade zinc SELENIDE (cas 22541-48-6) by the reactive diffusive process07/14/2019

The preparation of infrared windows grade zinc selenide (ZnSe) by the reactive diffusion process between liquid zinc and selenium was the goal of present work. In this regards, high purity zinc and Se elements with a nominal composition of Zn50Se50 were capsulated in quartz ampoule and annealed ...detailed

22541-48-6Relevant articles and documents

Novel organotin complexes derived from 2,2′-selenodiacetic acid: Synthesis and biological evaluation

Li, Qianli,Liu, Xinglong,Cheng, Shuang,Zhang, Rufen,Shi, Yang,Ma, Chunlin

, p. 32484 - 32492 (2016)

The reactions of 2,2′-selenodiacetic acid and the corresponding organotin(iv) chloride with sodium ethoxide in ethanol, or via a solvothermal synthetic route, have afforded four organotin polymers, namely, [(Me3Sn)2Se(CH2COO)2]n (1), [(Me2Sn)2Se(CH2COO)2(μ3-O)]n (2), [(Bu3Sn)2Se(CH2COO)2]n (3), and [(Bu2Sn)Se(CH2COO)2]n (4). All the complexes were fully characterized by elemental analysis, FT-IR, NMR (1H, 13C, and 119Sn) spectroscopy and single crystal X-ray diffraction analysis. The structural analysis reveals that complex 1 is a 2D-polymer containing interconnected 24-membered (Sn4O8C10Se2) macrocyclic rings. Unlike complex 1, the 2D polymer structure of complex 2 is made up of the typical ladder tetraorganodistannoxane unit containing 32-membered (Sn4O8C16Se4) macrocyclic rings. Complex 3 is a 3D corrugated polymeric structure in which the deprotonated dicarboxylic acid acts as a tetradentate ligand by four oxygen atoms. Complex 4 is a 1D zigzag coordination polymer and the tin coordination geometry is described as skewed-trapezoidal bipyramidal. In particular, preliminary cytotoxic assessments of the involvement of complex 4 in the apoptotic death of MDA cells were conducted, and the results revealed that the antiproliferative and proapoptotic effect of complex 4 in MDA cells prominently contributed to the overload of intracellular ROS levels and the dysfunctional depolarization of mitochondrial membranes.

Electrochemical synthesis of organochalcogenides in aqueous medium

Ribeiro Neto, Pedro B.,Santana, Sonydelane O.,Levitre, Guillaume,Galdino, Danilo,Oliveira, Jadson L.,Ribeiro, Rogério T.,Barros, Maria E. S. B.,Bieber, Lothar W.,Menezes, Paulo H.,Navarro, Marcelo

supporting information, p. 657 - 661 (2016/02/12)

The electrochemical preparation of telluride, selenide and sulfide ions was carried out in NaOH aqueous solution, using a two compartment cell. Organochalcogenides were prepared from halogenated compounds in a two-step procedure. The monochalcogenides were obtained as the major products in good yields.

Ultrasound-Induced Electrochemical Synthesis of the Anions Se2(2-), Se(2-), Te2(2-), and Te(2-)

Gautheron, Bernard,Tainturier, Gerard,Degrand, Chantal

, p. 5579 - 5581 (2007/10/02)

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