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Se(Se)-phenyl 4-chlorodiselenoperbenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59502-03-3

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59502-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59502-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,0 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59502-03:
(7*5)+(6*9)+(5*5)+(4*0)+(3*2)+(2*0)+(1*3)=123
123 % 10 = 3
So 59502-03-3 is a valid CAS Registry Number.

59502-03-3Relevant academic research and scientific papers

Reactions of O-Silyl Selenocarboxylates; IR and NMR Spectra of Heteroatom-substituted Selenocarboxylates

Kageyama, Hideki,Kido, Kenji,Kato, Shinzi,Murai, Toshiaki

, p. 1083 - 1088 (2007/10/02)

O-Silyl selenocarboxylates 1 react readily with acyl chlorides to give selenoanhydrides.Attempts to synthesize unsymmetrical selenoanhydrides selectively gave mixtures of the desired products with symmetrical selenoanhydrides.Ph3GeCl, Ph3SnCl, Ph3PbCl, Ph

Triorganogermanium Selenocarboxylates: Synthesis and Reactions

Kato, Shinzi,Ibi, Kazumasa,Kageyama, Hideki,Ishihara, Hideharu,Murai, Toshiaki

, p. 558 - 562 (2007/10/02)

A series of triphenylgermanium selenocarboxylates 3 were synthesized and characterized.The esters 3 are thermally stable, but labile towards moisture and oxygen.They react with arenesulfenyl chlorides and areneselenenyl bromides at room temperature to afford the corresponding acyl arenesulfenyl selenides and acyl aryl diselenides in moderate yields. Keywords: Triorganogermanium Selenocarboxylates, Aroyl Aryl Diselenides, Aroyl Arenesulfenyl Selenides

Isolation and characterization of Se-organolead selenocarboxylates

Kato, Shinzi,Ishihara, Hideharu,Ibi, Kazumasa,Kageyama, Hideki,Murai, Toshiaki

, p. 313 - 320 (2007/10/02)

Se-organolead selenocarboxylates were characterized after they were obtained from the reactions of alkali metal or piperidinium selenocarboxylates with organolead chlorides in moderate to good yields.The reactions of triphenyllead selenocarboxylates with

A Convenient Preparation of Aryl Arylcarbonyl Diselenides

Ishihara, Hideharu,Matsunami, Nobuaki,Yamada, Yukihiro

, p. 371 - 373 (2007/10/02)

A novel method for the synthesis of aryl arylcarbonyl diselenides via the reaction of potassium areneselenocarboxylates with areneselenenyl bromides is described.

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