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2-((E)-1-Methoxy-3-phenyl-allyl)-cyclohex-2-enone is a complex organic compound characterized by a cyclohexenone ring, which is a six-membered carbon ring with a double bond and a ketone group. The compound features a methoxy group (-OCH3) attached to the allyl chain, which is in the E configuration, indicating the geometric arrangement of the double bond. The allyl chain is connected to a phenyl group (C6H5), which adds aromatic character to the molecule. This chemical structure is significant in organic chemistry, potentially serving as an intermediate in the synthesis of various pharmaceuticals, fragrances, or other specialty chemicals. The specific arrangement of functional groups and the E configuration of the double bond influence its reactivity and potential applications in chemical transformations.

78905-89-2

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78905-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78905-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,0 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78905-89:
(7*7)+(6*8)+(5*9)+(4*0)+(3*5)+(2*8)+(1*9)=182
182 % 10 = 2
So 78905-89-2 is a valid CAS Registry Number.

78905-89-2Downstream Products

78905-89-2Relevant academic research and scientific papers

An efficient and rapid chalcogenide-Morita-Baylis-Hillman process promoted by TBDMSOTf and a thiolane

Rao, Jamjanam Srivardhana,Brière, Jean-Fran?ois,Metzner, Patrick,Basavaiah, Deevi

, p. 3553 - 3556 (2007/10/03)

The ability of the combination of sulfide/TBDMSOTf to promote a chalcogenide-Morita-Baylis-Hillman reaction is reported. The original Michael-Mukaiyama-retroaldol sequence took place and furnished the MBH adducts from the corresponding enones and acetals.

A simple procedure for α-alkoxyalkylation of α,β-enones via pyridiniosilylation

Kim,Kim,Park

, p. 2043 - 2044 (2007/10/02)

A one-pot, three-step procedure for α-alkoxyalkylation of α,β-enones utilizing a new pyridiniosilylation reaction is described.

TRIMETHYLSILYL TRIFLATE IN ORGANIC SYNTHESIS

Noyori, R.,Murata, S.,Suzuki, M.

, p. 3899 - 3910 (2007/10/02)

Trimethylsilyl triflate is a powerful silylating agent for organic compounds and acts as a catalyst which accelerates a variety of nucleophilic reactions in aprotic media.The reactions proceed via one-center, electrophilic coordination of the silyl group to hetero functional groups and exhibit unique selectivities.

A NEW PROCEDURE FOR α-ALKOXYALKYLATION OF α,β-UNSATURATED KETONES

Suzuki, M.,Kawagishi, T.,Noyori, R.

, p. 1809 - 1812 (2007/10/02)

A one-pot procedure for α-alkoxyalkylation of α,β-unsaturated ketoneshas been devised, which by combination with the organocopper conjugate addition reaction provides a new tool for vicinal carba-condensation of enones.

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