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(3-phenoxyprop-1-ynyl)(phenyl)tellane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1046490-89-4

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1046490-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1046490-89-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,4,9 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1046490-89:
(9*1)+(8*0)+(7*4)+(6*6)+(5*4)+(4*9)+(3*0)+(2*8)+(1*9)=154
154 % 10 = 4
So 1046490-89-4 is a valid CAS Registry Number.

1046490-89-4Downstream Products

1046490-89-4Relevant academic research and scientific papers

Cesium hydroxide-catalyzed reaction of terminal alkynes with diarylditellurides to synthesize alkynyl tellurides

Zou, Kang Bing,Qiu, Ren Hua,Fang, Da Wei,Liu, Xin You,Xu, Xin Hua

, p. 2237 - 2242 (2008)

In the presence of a catalytic amount of cesium hydroxide under an air atmosphere, the reaction of diarylditellurides (1.0 mmol) with terminal alkynes (2.2 mmol) at room temperature exclusively give alkynyl tellurides in good yields. Copyright Taylor & Fr

Bronsted acid catalyzed intramolecular hydroarylation for the synthesis of cycloalkenyl selenides and tellurides

Eom, Dahan,Park, Sangjune,Park, Youngchul,Lee, Kooyeon,Hong, Gilbert,Lee, Phil Ho

, p. 2672 - 2682 (2013/06/04)

Trifluoromethanesulfonic acid catalyzed intramolecular hydroarylation of alkynyl selenides and tellurides is developed for the preparation of cycloalkenyl selenide and telluride derivatives through a selective 6- and 7-endo mode. The cycloalkenyl selenides and tellurides can be easily converted into a wide range of other valuable functionalities, including cyclic olefins, allylic alcohols, enynes, 1,3-dienes, and α,β-unsaturated aldehydes. Trifluoromethanesulfonic acid catalyzed intramolecular hydroarylation of alkynyl selenides and tellurides is developed for the preparation of cycloalkenyl selenide and telluride derivatives through a selective 6- and 7-endo mode. The cycloalkenyl selenides and tellurides can be easily converted into a variety of valuable functionalities, including cyclic olefins, allylic alcohols, enynes, 1,3-dienes, and α,β-unsaturated aldehydes. Copyright

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