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Benzene, [(1-phenylethenyl)seleno]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61634-68-2

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61634-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61634-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,3 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61634-68:
(7*6)+(6*1)+(5*6)+(4*3)+(3*4)+(2*6)+(1*8)=122
122 % 10 = 2
So 61634-68-2 is a valid CAS Registry Number.

61634-68-2SDS

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 1-phenylethenylselanylbenzene

1.2 Other means of identification

Product number -
Other names -

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:61634-68-2 SDS

61634-68-2Downstream Products

61634-68-2Relevant academic research and scientific papers

A simple and general preparation of vinylic sulfides, selenides and tellurides

Silveira, Claudio C.,Santos, Paulo Cesar S.,Mendes, Samuel R.,Braga, Antonio L.

scheme or table, p. 3787 - 3790 (2009/04/06)

A general method for the synthesis of vinylic chalcogenides by nucleophilic and Ni-catalyzed vinylic substitution on vinylic halides by phenyl chalcogenolates is described. The reactions were regio and stereoselective for the nickel catalyzed substitution

Synthesis of chalcogenides using indium intermediates in aqueous media

Galindo, Andréa C.,Oliveira, Juliana M.,Barboza, Maria A. G.,Gon?alves, Simone M. C.,Menezes, Paulo H.

, p. 129 - 140 (2007/10/03)

Selenides and vinylic selenides were synthesized from their corresponding organic halides and alkynes in aqueous media using indium metal.

Palladium(0)-catalyzed regio- and stereoselective addition of heteroatom compounds bearing Si-Se, Ge-Se, and Si-Ge bonds to phenylacetylene

Ogawa, Akiya,Kuniyasu, Hitoshi,Takeba, Mitsuhiro,Ikeda, Takuma,Sonoda, Noboru,Hirao, Toshikazu

, p. 1 - 4 (2007/10/03)

A novel palladium(0)-catalyzed addition of a silyl selenide (1, Me3SiSePh) to phenylacetylene proceeds regio- and stereoselectively to give (Z)-1-phenylseleno-2(trimethylsilyl)styrene (2). Similarly, a germyl selenide (3, Me3GeSePh) adds to phenylacetylene with excellent regio- and stereoselectivity.

Regiospecific hydroselenation of terminal acetylenes using aluminum phenylselenolate anions

Dabdoub, Miguel J.,Cassol, Tania M.,Batista, Antonio C. F.

, p. 9005 - 9008 (2007/10/03)

Regiospecific hydroselenation of terminal acetylenes using aluminum phenylselenolates afforded the 1-organyl-1-phenylseleno ethenes in good yields. The first example of exclusive formation of the hydroselenation Markovnikov adducts is described. Copyright

The first example of transitionmetal-catalyzed hydroselenation of acetylenes

Kuniyasu, Hitoshi,Ogawa, Akiya,Sato, Ken-Ichiro,Ryu, Iihyong,Sonoda, Noboru

, p. 5525 - 5528 (2007/10/02)

A variety of transition metal complexes catalyzed the regioselective hydroselenation of acetylenes. In particular, the palladium acetate-catalyzed reaction afforded the Markovnikov adducts with high selectivity.

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