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Sodium selenide, with the chemical formula Na2Se, is a highly toxic and reactive chemical compound. It is typically found as a yellow-orange crystalline solid and is known for its use in various applications due to its unique properties.

1313-85-5

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1313-85-5 Usage

Uses

Used in Chemical Synthesis:
Sodium selenide is used as a reagent in chemical reactions for the preparation of organoselenium compounds. Its reactivity allows for the formation of a wide range of organoselenium compounds, which have diverse applications in various industries.
Used in Semiconductor Production:
In the electronics industry, sodium selenide is utilized in the production of semiconductors. Its properties make it a valuable component in the manufacturing process, contributing to the development of advanced electronic devices.
Used in Medical Applications:
Sodium selenide finds use in some medical applications, such as cancer therapy and imaging. Its unique properties allow it to play a role in the diagnosis and treatment of certain medical conditions. However, due to its highly toxic nature, it must be handled with extreme caution to prevent adverse effects.
Used in Cancer Therapy:
In the field of oncology, sodium selenide is employed as a potential therapeutic agent. Its ability to target and affect cancer cells makes it a candidate for further research and development in cancer treatment.
Used in Imaging Techniques:
Sodium selenide is also utilized in medical imaging techniques, where its properties can enhance the visualization of internal structures and assist in the diagnosis of various conditions.
It is crucial to note that due to the highly toxic nature of sodium selenide, proper safety precautions must be taken when handling and using Sodium selenide. Exposure can cause severe irritation, burns, and systemic toxicity if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 1313-85-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,1 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1313-85:
(6*1)+(5*3)+(4*1)+(3*3)+(2*8)+(1*5)=55
55 % 10 = 5
So 1313-85-5 is a valid CAS Registry Number.
InChI:InChI=1/2Na.Se/rNa2Se/c1-3-2

1313-85-5 Well-known Company Product Price

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  • Alfa Aesar

  • (36187)  Sodium selenide, 99.8% (metals basis)   

  • 1313-85-5

  • 1g

  • 3452.0CNY

  • Detail
  • Alfa Aesar

  • (36187)  Sodium selenide, 99.8% (metals basis)   

  • 1313-85-5

  • 5g

  • 15552.0CNY

  • Detail

1313-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium selenide

1.2 Other means of identification

Product number -
Other names Sodium Selenide

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:1313-85-5 SDS

1313-85-5Synthetic route

selenium
7782-49-2

selenium

sodium tetrahydroborate
16940-66-2

sodium tetrahydroborate

sodium selenide
1313-85-5

sodium selenide

Conditions
ConditionsYield
In water Inert atmosphere; Schlenk technique;
sodium selenide
1313-85-5

sodium selenide

2,4,6-trimethylphenyl diazonium chloride
70335-45-4

2,4,6-trimethylphenyl diazonium chloride

bis(2,4,6-trimethylphenyl) selenide
142073-25-4

bis(2,4,6-trimethylphenyl) selenide

Conditions
ConditionsYield
In water at 40℃; for 3h; Inert atmosphere; Schlenk technique;60%

1313-85-5Relevant academic research and scientific papers

Cyclopalladation of dimesityl selenide: Synthesis, reactivity, structural characterization, isolation of an intermediate complex with C-H...Pd intra-molecular interaction and computational studies

Kolay, Siddhartha,Wadawale, Amey,Das, Dasarathi,Kisan, Hemanta K.,Sunoj, Raghavan B.,Jain, Vimal K.

supporting information, p. 10828 - 10837 (2013/09/12)

The reaction of dimesityl selenide (Mes2Se) with either PdCl2(PhCN)2 in toluene or PdCl2 in toluene-acetonitrile yields a chloro-bridged binuclear palladium complex, [Pd2Cl2(μ-Cl)2(Mes2Se) 2] (1), whereas with Na2PdCl4 in refluxing ethanol, a cyclometallated palladium complex, [Pd2(μ-Cl) 2{MesSeC6H2(Me2)CH2} 2] (2) is afforded. 2 can also be obtained when 1 is refluxed in ethanol. On treatment with Pb(Epy)2 in dichloromethane, 2 afforded the Epy-bridged binuclear complexes, [Pd2(μ-Epy) 2{MesSeC6H2(Me2)CH2} 2] (3; E = S (3a) or Se (3b)). Treatment of 2 with PPh3 yields a bridge-cleaved monomeric complex, [PdCl{MesSeC6H 2(Me2)CH2}(PPh3)]. The molecular structures of 1-3 were established by X-ray diffraction analyses. All the complexes are dimeric, with the palladium atoms acquiring a distorted square planar configuration. There are intra-molecular C-H...Pd interactions (dM-H: 2.75 A and 3) bond leading to metallation. The optimized geometry of 1 obtained using the DFT(B3LYP) computational method identified a C-H...Pd contact distance of 2.78 A. There are two independent molecules of 2 in the unit cell, which differ slightly in bond lengths, bond angles and torsion angles. The mechanism of formation of the dimeric species 2 is examined using DFT (B3LYP) computations. The Royal Society of Chemistry 2013.

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