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2-allyl-1-bromo-4-(trifluoromethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869725-65-5

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869725-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869725-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,7,2 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 869725-65:
(8*8)+(7*6)+(6*9)+(5*7)+(4*2)+(3*5)+(2*6)+(1*5)=235
235 % 10 = 5
So 869725-65-5 is a valid CAS Registry Number.

869725-65-5Relevant academic research and scientific papers

Relay catalysis: Enantioselective synthesis of cyclic benzo-fused homoallylic alcohols by chiral bronsted acid-catalyzed allylboration/ring closing metathesis

Fustero, Santos,Rodriguez, Elsa,Lazaro, Ruben,Herrera, Lidia,Catalan, Silvia,Barrio, Pablo

supporting information, p. 1058 - 1064 (2013/05/21)

Six- and seven-membered benzo-fused cyclic homoallylic alcohols can be readily synthesized by a tandem chiral Bronsted acid-catalyzed allyl (crotyl)boration/ring closing metathesis sequence performed under orthogonal relay catalysis conditions. Excellent enantio- and diastereoselectivities are obtained in most of the cases. In addition, the parent crotylboration/RCM process is also described. The required substrates, ortho-vinylbenzaldehydes, are readily available in one step from commercially available starting materials. Both catalysts and reactants are also available from commercial suppliers. The reaction shows broad functional group compatibility and is also suitable for heteroaromatic substrates. Substitution at any position of the aromatic ring is tolerated; however, substitution at position 6 results in a substantial drop in enantioselectivity. Copyright

Piperazinylpiperidine derivatives as chemokine receptor antagonists

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Page/Page column 28, (2008/06/13)

The present invention relates to compounds of Formula I: wherein variable substituents are defined herein, that modulate the activity of or bind to chemokine receptors such as CCR5. In some embodiments, the compounds of the invention are selective for CCR

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