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Methyl-1-phenyl-2-cyclohexen-2,3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54780-60-8

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54780-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54780-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54780-60:
(7*5)+(6*4)+(5*7)+(4*8)+(3*0)+(2*6)+(1*0)=138
138 % 10 = 8
So 54780-60-8 is a valid CAS Registry Number.

54780-60-8Downstream Products

54780-60-8Relevant academic research and scientific papers

Reaction of benzyne with cyclic olefins-II. Ene addition to some cycloalkenes

Mehta,Singh, B.Pal

, p. 2409 - 2412 (1974)

Addition of benzyne to 1-methylcyclohexene, (+)-carvomenthene, (+)-limonene, α- and β-pinenes and δ3-carene has been investigated. Structures to the ene products formed are assigned on the basis of spectroscopic evidence. Arguments are advanced in favour of a concerted ene mechanism for the addition of benzyne to these olefins.

Rhodium-Catalyzed Enantioconvergent Isomerization of Homoallylic and Bishomoallylic Secondary Alcohols

Huang, Rui-Zhi,Lau, Kai Kiat,Li, Zhaofeng,Liu, Tang-Lin,Zhao, Yu

, p. 14647 - 14654 (2018/11/06)

We present herein an unprecedented enantioselective isomerization of homoallylic and bishomoallylic secondary alcohols, catalyzed by a commercially available rhodium-complex and a base. This catalytic redox-neutral process provides an effective access to chiral ketones in high efficiency and enantioselectivity, without the use of any stoichiometric reagent or generation of any waste. For the reaction of homoallylic alcohols, this system achieved not only a stereoconvergent access to chiral ketones bearing a β-stereocenter (up to 95%, 86% ee) but also a concomitant oxidative kinetic resolution of the alcohol substrates (S > 20). In the case of bishomoallylic alcohols, an intriguing ligand-induced divergent reactivity was observed. A terminal-to-internal alkene isomerization promoted by Rh/L7 followed by redox isomerization using Rh/BINAP system produced chiral ketones bearing a γ-stereocenter with high yield and enantioselectivity. Mechanistic studies provided strong support for the redox-isomerization pathway with chain walking of the key alkyl-Rh intermediate.

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