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diselane-1,2-diylbis(phenylmethanone) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38572-13-3

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38572-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38572-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38572-13:
(7*3)+(6*8)+(5*5)+(4*7)+(3*2)+(2*1)+(1*3)=133
133 % 10 = 3
So 38572-13-3 is a valid CAS Registry Number.

38572-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Se-benzoylselanyl benzenecarboselenoate

1.2 Other means of identification

Product number -
Other names Bis(benzoyl) diselenide

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:38572-13-3 SDS

38572-13-3Relevant academic research and scientific papers

Samarium diiodide-induced reduction of elemental selenium leading to a selenolate anion species. A selective synthesis of diacyl diselenides

Jia,Zhang,Zhou

, p. 1403 - 1408 (1993)

Elemental selenium was reduced by samarium diiodide in THF to produce selenolate anion species which reacted with acyl chlorides to give diacyl diselenides in good yields under mild and neutral conditions.

Synthesis of sodium diselenides and its reaction with benzoyl chloride under phase transfer catalysis and microwave irradiation conditions

Wang, Jin-Xian,Bai, Lin,Liu, Zhanxiang

, p. 971 - 977 (2000)

A simple, fast and efficient procedure for the synthesis of dibenzoyl diselenides involves the reaction of selenium with sodium hydroxide under phase transfer catalysis and microwave irradiation conditions to give sodium diselenides, which reacts with ben

Radical-Cascade Avenue for 3,4-Fused-Ring-Substituted Thiophenes

Agrawal, Abhijeet R.,Kumar, Neha Rani,Debnath, Sashi,Das, Sarasija,Kumar, Chandan,Zade, Sanjio S.

, p. 4728 - 4731 (2018/08/23)

A single-step intramolecular radical cascade reaction of diynes and thioacetic acid in the presence of a catalytic amount of azobis(isobutyronitrile) as a radical initiator has been developed to synthesize thiophenes. This method allows easy and effective construction of a thiophene scaffold having 3,4-fused-ring substitution and unsubstituted 2,5-positions for further functionalization and polymerization. Using this method, derivatives of cyclopenta[c]thiophene, 3,4-ethylenedioxythiophene, and thiophene-containing spirocyclic compound have been synthesized.

Synthesis and characterization of novel organic heteroatom compounds from reaction of Woollins' reagent with various organic substrates

Hua, Guoxiong,Du, Junyi,Cordes, David B.,Arachchige, Kasun S. A.,Slawin, Alexandra M. Z.,Woollins, J. Derek

supporting information, p. 341 - 346 (2016/04/05)

A series of new selenium-containing heteroatom compounds were synthesized in good yields by the reaction of Woollins reagent with various organic substrates such as cyclohexylamine, N-benzoylbenzamide, benzoic anhydride, 4-fluoro-N-(2-oxo-2-phenylethyl)benzamide, N-benzoylbenzamide, benzoic anhydride, 3-(bromomethyl)benzonitrile, 1,2-diphenylethane-1,2-diol, and sodium alcoholate. Three representative X-ray structures are described.

Organoselenosilane-mediated selective mild access to selenolesters, selenoanhydrides and diacyl diselenides

Capperucci, Antonella,Deglinnocenti, Alessandro,Tiberi, Caterina

experimental part, p. 2248 - 2252 (2011/10/31)

Reaction of acyl chlorides with phenylselenotrimethyl-silane promoted by TBAF afforded a mild general access to selenolesters in good yields. When acyl chlorides were reacted with bis(trimethylsilyl)selenide (HMDSS) in 2:1 or 1:1 ratio a selective entry t

Lithium aluminum hydride-based selenating reagent and preparation methods using same

-

, (2008/06/13)

A selenating reagent obtained by reacting lithium aluminum hydride with selenium powder in an organic solvent. In addition, a method for preparing a selenating reagent includes reacting lithium aluminum hydride with selenium powder in an organic solvent.

Improved solubility and stability of trialkylammonium selenocarboxylate in organic solvents for efficient amidation with azides

Surabhi, Prathima,Wu, Xinghua,Hu, Longqin

, p. 4609 - 4613 (2007/10/03)

Trialkylammonium selenocarboxylate, formed in situ from the reaction of diacyl diselenide with piperidine in the presence of diisopropylethylamine, was found to react readily at room temperature with electron-deficient azides to form amides in excellent yields. The trialkylammonium selenocarboxylate salt formed has good solubility and stability in organic solvents. The enhanced stability allowed mild heating to improve the amidation yields with electron-rich azides.

Reactions of acyl chlorides with LiAlHSeH. Preparation of diacyl selenides, diacyl diselenides, selenocarboxylates and cyclic selenoanhydrides

Koketsu, Mamoru,Nada, Futoshi,Hiramatsu, Sohma,Ishihara, Hideharu

, p. 737 - 740 (2007/10/03)

Various diacyl selenides, diacyl diselenides and selenocarboxylates were synthesized by reaction of several acyl chlorides with LiAlHSeH. Reaction of diacyl chloride with LiAlHSeH afforded cyclic selenoanhydrides. In the 77Se NMR spectra, we fo

Efficient Synthesis of Selenocarbonyl Compounds by Treating Carbonyl Compounds with Bis(1,5-cyclooctanediylboryl) Selenide

Shimada, Kazuaki,Jin, Norikazu,Kawaguchi, Michiko,Dobashi, Kumiko,Nagano, Yumi,Fujimura, Manabu,Kudoh, Eiichi,Kai, Tomonari,Saito, Noboru,Masuda, Jun-Ichi,Iwaya, Masaki,Fujisawa, Hiroyuki,Aoyagi, Shigenobu,Takikawa, Yuji

, p. 197 - 206 (2007/10/03)

Selenoaldehydes and selenoketones were generated in situ, by treating aldehydes or ketones, respectively, with bis(1,5-cyclooctanediylboryl) selenide; the resulting selenocarbonyl compounds were trapped with 2,3-dimethyl-1,3-butadiene to give the correspo

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