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[4-((Z)-1,2-Diphenyl-vinyl)-phenyl]-dimethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102459-17-6

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102459-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102459-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,5 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102459-17:
(8*1)+(7*0)+(6*2)+(5*4)+(4*5)+(3*9)+(2*1)+(1*7)=96
96 % 10 = 6
So 102459-17-6 is a valid CAS Registry Number.

102459-17-6Downstream Products

102459-17-6Relevant academic research and scientific papers

Stereoselective synthesis of trisubstituted alkenes via cobalt-catalyzed double dehydrogenative borylations of 1-alkenes

Wen, Huanan,Zhang, Lei,Zhu, Suzhen,Liu, Guixia,Huang, Zheng

, p. 6419 - 6425 (2017)

A highly selective cobalt-catalyzed single and double dehydrogenative borylations (DHBs) of terminal alkenes have been developed for the synthesis of trans-monoborylalkenes and diborylalkenes, respectively. While the cobalt-catalyzed double DHBs of aryl 1

A decarboxylative approach for regioselective hydroarylation of alkynes

Zhang, Jing,Shrestha, Ruja,Hartwig, John F.,Zhao, Pinjing

, p. 1144 - 1151 (2016/11/28)

Regioselective activation of aromatic C-H bonds is a long-standing challenge for arene functionalization reactions such as the hydroarylation of alkynes. One possible solution is to employ a removable directing group that activates one of several aromatic C-H bonds. Here we report a new catalytic method for regioselective alkyne hydroarylation with benzoic acid derivatives during which the carboxylate functionality directs the alkyne to the ortho-C-H bond with elimination in situ to form a vinylarene product. The decarboxylation stage of this tandem sequence is envisioned to proceed with the assistance of an ortho-alkenyl moiety, which is formed by the initial alkyne coupling. This ruthenium-catalysed decarboxylative alkyne hydroarylation eliminates the common need for pre-existing ortho-substitution on benzoic acids for substrate activation, proceeds under redox-neutral and relatively mild conditions, and tolerates a broad range of synthetically useful aromatic functionality. Thus, it significantly increases the synthetic utility of benzoic acids as easily accessible aromatic building blocks.

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