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2-Cyclohexen-1-one, 2-(bromomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

927434-10-4

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927434-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 927434-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,7,4,3 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 927434-10:
(8*9)+(7*2)+(6*7)+(5*4)+(4*3)+(3*4)+(2*1)+(1*0)=174
174 % 10 = 4
So 927434-10-4 is a valid CAS Registry Number.

927434-10-4Upstream product

927434-10-4Relevant academic research and scientific papers

A Metal-Free Synthesis of 2-Alkyl(or Aryl) Thiomethyl-2-cyclohexenones from Cyclic Morita–Baylis–Hillman Bromides

Baioui, Narjes,Abidi, Ahlem,Rezgui, Farhat

, p. 704 - 709 (2016/09/20)

Under mild conditions, an efficient and rapid S-allylation of thiols with cyclic Morita–Baylis–Hillman (MBH) bromides without the need of a transition-metal catalyst or an expensive additive is described herein. Treatment of the MBH bromides with various

Transition-metal-free nucleophilic allylic substitutions of Morita–Baylis–Hillman bromides with aliphatic and aromatic amines

Baioui, Narjes,Elleuch, Haitham,Rezgui, Farhat

, p. 1796 - 1802 (2016/11/18)

A simple protocol for the preparation of functionalized allylic amines under mild, transition-metal-free conditions from the reaction of Morita–Baylis–Hillman (MBH) bromides with amines is described herein. The treatment of the MBH bromides with various amines in the presence of NaI and Et3N in aqueous acetone solution and at room temperature affords the corresponding functionalized allyl amines in moderate to good yields (45–87%). The reaction is rapid and carried out at room temperature.

The intramolecular reductive cyclization of cyclic enones

Handy, Scott T.,Omune, Duncan

, p. 1366 - 1371 (2007/10/03)

The reductive cyclization (electrohydrocyclization reaction) of tethered cyclic enones has been investigated under electrochemical, metal-mediated, and photochemical conditions. The tricyclic products are generally formed with excellent stereoselectivity,

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