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6-(3,3-Dimethyl-2-propenyl)-3-ethoxy-2-cyclohexenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58775-55-6

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58775-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58775-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,7 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58775-55:
(7*5)+(6*8)+(5*7)+(4*7)+(3*5)+(2*5)+(1*5)=176
176 % 10 = 6
So 58775-55-6 is a valid CAS Registry Number.

58775-55-6Relevant academic research and scientific papers

Synthetic Strategy for Construction of Highly Congested Tetracyclic Core (6-5-7-4) of Harziane Diterpenoids

Tu, Qian,Wang, Zheyuan,Zhang, Zhongchao,Huang, Jun,Yang, Zhen

, p. 4088 - 4093 (2021)

The structurally intriguing tetracyclic core of complex harziane diterpenoid was constructed in 14 steps from commercially available 3-ethoxycyclohex-2-en-1-one. The key steps were a Mn/Cu-mediated oxidative 1,3-dicarbonyl radical cascade cyclization reac

Total synthesis of (±)-garsubellin A

Kuramochi, Akiyoshi,Usuda, Hiroyuki,Yamatsugu, Kenzo,Kanai, Motomu,Shibasaki, Masakatsu

, p. 14200 - 14201 (2007/10/03)

The first total synthesis of garsubellin A, a neurotrophic compound with potent choline acetyltransferase-inducing activity, is described. Keys for success were (1) stereoselective intermolecular aldol reaction at the C-4 position with acetaldehyde, (2) stereoelective Claisen rearrangement to introduce an allyl group to the most sterically crowded position at C-6, (3) ring-closing metathesis to construct the B-ring, and (4) Wacker-type oxidative C-ring formation. This synthetic route can be extended to an asymmetric synthesis of garsubellin A using the Koga catalytic enantioselective alkylation, which produced enantioenriched α-prenyl cyclohexenone with excellent enantioselectivity (95% ee). Copyright

Pyrazolopyridine cycloalkanones and process for their preparation

-

, (2008/06/13)

Novel tetrahydropyrazolo-[3,4-b]quinolinones, cyclopenta[b]pyrazolo-[4,3-e]pyridinones and cyclohepta[b]-pyrazolo[4,3-e]pyridinones, useful as anxiolytics having reduced side effects, are disclosed, including methods of preparation, pharmaceutical compositions containing them and intermediates used in their preparation.

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