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(+/-)-[(1S,5R)-2-methyl-5-(1-methylvinyl)cyclohex-2-enyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84565-69-5

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84565-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84565-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,6 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84565-69:
(7*8)+(6*4)+(5*5)+(4*6)+(3*5)+(2*6)+(1*9)=165
165 % 10 = 5
So 84565-69-5 is a valid CAS Registry Number.

84565-69-5Downstream Products

84565-69-5Relevant academic research and scientific papers

Nickel-Catalyzed Arylation of C(sp3)-O Bonds in Allylic Alkyl Ethers with Organoboron Compounds

Li, Xiaowei,Li, Yuxiu,Zhang, Zhong,Shi, Xiaolin,Liu, Ruihua,Wang, Zemin,Li, Xiangqian,Shi, Dayong

, p. 6612 - 6616 (2021/09/02)

A nickel-catalyzed cross-coupling of allylic alkyl ethers with organoboron compounds through the cleavage of the inert C(sp3)-O(alkyl) bonds is described. Several types of allylic alkyl ethers can be coupled with various boronic acids or their derivatives to give the corresponding products in good to excellent yields with wide functional group tolerance and excellent regioselectivity. The gram-scale reaction and late-stage modification of biologically active compounds further prove the practicality of this synthetic method.

Efficient palladium-catalyzed nucleophilic addition of triorganoindium reagents to carbocyclic derivatives

Baker, Lucas,Minehan, Thomas

, p. 3957 - 3960 (2007/10/03)

Palladium (0)-catalyzed allylic substitution reactions employing triorganoindium reagents have been investigated. In situ generated vinyl- and arylindiums react with substituted and unsubstituted cyclohex-2-enyl esters in the presence of 1-3 mol % Pd2(dba)3 to produce vinyl- or arylcyclohexenes in moderate to excellent yields. The stereoselectivity of this process was also examined, and evidence is presented that the reaction proceeds with inversion of stereochemical configuration.

A HYBRID BIRCH-CLAISEN METHODOLOGY FOR ARYLATION AT ALLYLIC TERMINI: SYNTHESIS OF (+/-)-HERBERTENE

Chandrasekaran, S.,Turner, John V.

, p. 3799 - 3802 (2007/10/02)

A hybrid Birch-Claisen methodology has been developed for the regio- and stereo-controlled arylation of allyl groups, and applied to a synthesis of (+/-)-herbertene.

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