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2-cyclohexenyl-1,3,5-trimethylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133039-16-4

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133039-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133039-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,3 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133039-16:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*9)+(2*1)+(1*6)=94
94 % 10 = 4
So 133039-16-4 is a valid CAS Registry Number.

133039-16-4Downstream Products

133039-16-4Relevant academic research and scientific papers

Bimolecular vinylation of arenes by vinyl cations

Bour, Christophe,Gandon, Vincent,Li, Zhilong

, p. 6507 - 6510 (2020)

Styrene derivatives can be easily synthesized from vinyl triflates and arenes under mild reaction conditions, using [Li][Al(OC(CF3)3)4] as a catalyst and LiHMDS as a base. This transformation is likely to involve a vinyl cation intermediate as an electrophile, which is corroborated by DFT calculations, deuterium-labeling and other control experiments. The use of an inert weakly coordinating anion is a decisive factor in this bimolecular vinylation process. This journal is

Well-defined air-stable palladium HASPO complexes for efficient Kumada-Corriu cross-couplings of (Hetero)aryl or alkenyl tosylates

Ackermann, Lutz,Kapdi, Anant R.,Fenner, Sabine,Kornhaab, Christoph,Schulzke, Carola

supporting information; experimental part, p. 2965 - 2971 (2011/05/05)

Palladium complexes of representative heteroatom-substituted secondary phosphine oxide (HASPO) preligands were synthesized and fully characterized, including X-ray crystal structure analysis. Importantly, these well-defined complexes served as highly efficient catalysts for Kumada-Corriu cross-coupling reactions of aryl, alkenyl, and even heteroaryl tosylates. Particularly, an air-stable catalyst derived from inexpensive PinP(O)H displayed a remarkably high catalytic efficacy, which resulted in cross-couplings at low catalyst loadings under exceedingly mild reaction conditions with ample scope.

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