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56592-98-4

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56592-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56592-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,9 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56592-98:
(7*5)+(6*6)+(5*5)+(4*9)+(3*2)+(2*9)+(1*8)=164
164 % 10 = 4
So 56592-98-4 is a valid CAS Registry Number.

56592-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(butan-2-yldiselanyl)butane

1.2 Other means of identification

Product number -
Other names dibutan-2-yldiselane

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:56592-98-4 SDS

56592-98-4Downstream Products

56592-98-4Relevant academic research and scientific papers

Synthesis of selenocystine derivatives from cystine by applying the transformation reaction from disulfides to diselenides

Iwaoka, Michio,Haraki, Chie,Ooka, Ryuta,Miyamoto, Masahiro,Sugiyama, Ai,Kohara, Yumiko,Isozumi, Noriyoshi

, p. 3861 - 3863 (2007/10/03)

A stepwise conversion of a disulfide (SS) to a diselenide (SeSe) bond through the corresponding iodide intermediate was implemented and was applied to the synthesis of selenocystamine and l-selenocystine derivatives from cystamine and l-cystine, respectively, in moderate yields.

Highly efficient route to diselenides from the reactions of imines and selenium in the presence of carbon monoxide and water

Zhao, Xiaodan,Yu, Zhengkun,Zeng, Fanlong,Chen, Jinzhu,Wu, Xiaowei,Wu, Sizhong,Xiao, Wen-Jing,Zheng, Zhaoyan

, p. 877 - 882 (2007/10/03)

Reactions of selenium with imines (RR1C=NR2) of aldehydes and ketones in the presence of carbon monoxide, water and triethylamine lead to reductive selenation, on aerobic work-up, to afford symmetrical diselenides (RR1CHSe)2 in good to excellent yields. The proposed mechanism suggests that both in situ generated carbonyl selenide (SeCO) and hydrogen selenide (H2Se) are involved in the reaction.

Condition-driven selective syntheses of dialkyl diselenides involving elemental selenium and sodium borohydride

Krief, Alain,Derock, Michel

, p. 1012 - 1014 (2007/10/03)

Dialkyl diselenides have been prepared from alkyl halides, sodium borohydride and elemental selenium using two different methods. One of them involves the intermediate formation of diselenide dianion equivalent ( -SeSe-).

Synthesis of diselenides and selenides from elemental selenium

Krief, Alain,Derock, Michel

, p. 3083 - 3086 (2007/10/03)

Sodium hydride is able to reduce elemental selenium to sodium diselenide (Na2Se2), but not to sodium selenide (Na2Se). Dialkyl diselenides and even dialkyl selenides, including unsymmetrical dialkyl selenides, can be nevertheless synthesized using the proper Se/NaH ratio (1/1 or 1/2).

The first synthesis of organic diselenolates: Application to the synthesis of diorganyl diselenides

Krief, Alain,Van Wemmel, Thierry,Redon, Martine,Dumont, Willy,Delmotte, Cathy

, p. 2245 - 2247 (2007/10/03)

The addition of elemental selenium to organolithium compounds 1 or organic selenates 2 gives organic diselenolates 3. The reactions proceed by the insertion of two selenium atoms into the carbon-metal bonds or of one selenium atom into a selenolate. Evidence for the existence of n- butyldisilenol has also been obtained.

Synthesis Utilizing Reducing Ability of Carbon Monoxide: A New Method for Selective Synthesis of Diorganyl Selenides and Diselenides Using a Selenium-Carbon Monoxide-Water Reaction System

Nishiyama, Yutaka,Katsuura, Akio,Negoro, Atsuhito,Hamanaka, Sawako,Miyoshi, Noritaka,et al.

, p. 3776 - 3780 (2007/10/02)

A new approach to the synthesis of diorganyl selenides and diselenides is described.Selective generation of tertiary amine salts of hydrogen selenide (->*+>) and hydrogen diselenide (->*+>) ha

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