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(E)-2-(3-methoxy-phenylmethylene)-cyclohexanone is a complex organic compound characterized by a cyclohexanone core, which is a six-membered carbon ring with a ketone group (C=O) at the 2-position. The compound features a 3-methoxy-phenylmethylene group attached to the cyclohexanone through a double bond, indicating an E-configuration, which means the substituents are on opposite sides of the double bond. The 3-methoxy group on the phenyl ring introduces an ether linkage, enhancing the molecule's polarity. (E)-2-(3-methoxy-phenylmethylene)-cyclohexanone is likely to be used in the synthesis of pharmaceuticals, fragrances, or other specialty chemicals due to its unique structure and reactivity.

56005-42-6

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56005-42-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56005-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,0 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56005-42:
(7*5)+(6*6)+(5*0)+(4*0)+(3*5)+(2*4)+(1*2)=96
96 % 10 = 6
So 56005-42-6 is a valid CAS Registry Number.

56005-42-6Relevant academic research and scientific papers

Redox-Neutral Cobalt(III)-Catalyzed C-H Activation/Annulation of α,β-Unsaturated Oxime Ether with Alkyne: One-Step Access to Multisubstituted Pyridine

Mohanty, Smruti Ranjan,Pati, Bedadyuti Vedvyas,Banjare, Shyam Kumar,Das Adhikari, Gopal Krushna,Ravikumar, Ponneri Chandrababu

, p. 1074 - 1083 (2021/01/14)

A redox neutral Co(III)-catalyzed annulation of α,β-unsaturated oxime ether with alkyne has been reported. Multisubstituted pyridines were synthesized in good yields without the use of any heavy metal oxidants. The developed methodology tolerates a variety of functional groups. Notably, this transformation has been applied to the late-stage modification of the bioactive molecule dehydropregnenolone.

Ruthenium-catalysed synthesis of chiral exocyclic allylic alcoholsviachemoselective transfer hydrogenation of 2-arylidene cycloalkanones

Zhang, Kaili,Liu, Qixing,He, Renke,Chen, Danyi,Deng, Zhangshuang,Huang, Nianyu,Zhou, Haifeng

supporting information, p. 1628 - 1632 (2021/03/09)

An exclusive asymmetric reduction of C=O bonds of 2-arylidene four-, five-, six-, and seven-membered cycloalkanones has been studied systematically. The asymmetric transfer hydrogenation was performed using a robust and commercially available chiral diamine-derived ruthenium complex as a catalyst and HCOOH/Et3N as a hydrogen source under mild conditions, giving 51 examples of chiral exocyclic allylic alcohols in up to 96% yield and 99% ee. This method was also applicable to the gram-scale synthesis of the active intermediates of the anti-inflammatory loxoprofen and natural product (?)-goniomitine.

Highly Enantioselective Hydrogenation of α-Arylmethylene Cycloalkanones Catalyzed by Iridium Complexes of Chiral Spiro Aminophosphine Ligands

Xie, Jian-Bo,Xie, Jian-Hua,Liu, Xiao-Yan,Kong, Wei-Ling,Li, Shen,Zhou, Qi-Lin

supporting information; experimental part, p. 4538 - 4539 (2010/06/17)

The highly efficient asymmetric hydrogenation of α-arylmethylene cycloalkanones catalyzed by Ir-complexes of chiral spiro aminophosphine ligands was developed, providing chiral exo-cyclic allylic alcohols at high yields with excellent enantioselectivities (up to 97% ee) and high turnover numbers (S/C up to 10,000). This new reaction provided an efficient method for the synthesis of the key intermediate of the active form of the anti-inflammatory loxoprofen.

THE EFFECTS OF SUBSTITUENS AND SOLVENT POLARITY ON PHOTOCHEMICAL SIGMATROPIC SHIFTS. EXPERIMENTAL EVIDENCE IN FAVOUR OF THE OCCURRENCE OF SUDDEN POLARIZATION IN ACYCLIC ALKENES

Peijnenburg, W. J. G. M.,Buck, H. M.

, p. 4927 - 4940 (2007/10/02)

Furher experimental evidence regarding the occurence of sudden polarization in acyclic alkenes is presented.It is shown that the yield of formation of the product derived from an intramolecular photochemical -OH shift in the 1 is dependent only on the polarity of the solvent employed.This result could be well explained in terms of a stabilization of the zwitterionic intermediate formed upon irradiation of 1 by reorientation polarization of the dipole solvent molecules.Besides this, it was found that replacement of the alkyl group at the terminal carbon atom of the C3-C9 exocyclic double bond in 1 by a phenyl substituent led to the occurence of a photochemical -H shift.This directive effect of the substituents at the exocyclic double bond could be well explained on the basis of the sudden polarization model.

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